Canonical Allele Identifier: CA2578171321

Gene: LARP7

Linked Data

• gnomAD v4: 4-112646488-T-TTATAAAGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.112646489_112646490insATAAAGAAT , CM000666.2:g.112646489_112646490insATAAAGAAT	GRCh38
NC_000004.11:g.113567645_113567646insATAAAGAAT , CM000666.1:g.113567645_113567646insATAAAGAAT	GRCh37
NC_000004.10:g.113787094_113787095insATAAAGAAT	NCBI36
NG_032779.1:g.14526_14527insATAAAGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505034.6:c.303+38_303+39insATAAAGAAT	ENSP00000421541.2:n.303+38_303+39insATAAAGAAT
ENST00000505216.2:c.*62+38_*62+39insATAAAGAAT	ENSP00000424116.1:n.*62+38_*62+39insATAAAGAAT
ENST00000694891.1:c.303+38_303+39insATAAAGAAT	ENSP00000511571.1:n.303+38_303+39insATAAAGAAT
ENST00000694892.1:n.345_346insATAAAGAAT
ENST00000694893.1:n.434_435insATAAAGAAT
ENST00000694894.1:c.303+38_303+39insATAAAGAAT	ENSP00000511572.1:n.303+38_303+39insATAAAGAAT
ENST00000694895.1:c.303+38_303+39insATAAAGAAT	ENSP00000511573.1:n.303+38_303+39insATAAAGAAT
ENST00000694896.1:c.303+38_303+39insATAAAGAAT	ENSP00000511574.1:n.303+38_303+39insATAAAGAAT
ENST00000694897.1:c.303+38_303+39insATAAAGAAT	ENSP00000511575.1:n.303+38_303+39insATAAAGAAT
ENST00000694898.1:c.303+38_303+39insATAAAGAAT	ENSP00000511576.1:n.303+38_303+39insATAAAGAAT
ENST00000694899.1:c.303+38_303+39insATAAAGAAT	ENSP00000511577.1:n.303+38_303+39insATAAAGAAT
ENST00000694900.1:c.303+38_303+39insATAAAGAAT	ENSP00000511578.1:n.303+38_303+39insATAAAGAAT
ENST00000694901.1:c.*62+38_*62+39insATAAAGAAT	ENSP00000511579.1:n.*62+38_*62+39insATAAAGAAT
ENST00000694902.1:n.824+38_824+39insATAAAGAAT
ENST00000511529.2:c.303+38_303+39insATAAAGAAT	ENSP00000426376.2:n.303+38_303+39insATAAAGAAT
ENST00000512361.2:n.412+38_412+39insATAAAGAAT
ENST00000512589.6:c.*109+38_*109+39insATAAAGAAT	ENSP00000426709.1:n.*109+38_*109+39insATAAAGAAT
ENST00000684864.1:c.303+38_303+39insATAAAGAAT	ENSP00000509993.1:n.303+38_303+39insATAAAGAAT
ENST00000688617.1:n.577+38_577+39insATAAAGAAT
ENST00000689262.1:n.1454+38_1454+39insATAAAGAAT
ENST00000689844.1:c.303+38_303+39insATAAAGAAT	ENSP00000509899.1:n.303+38_303+39insATAAAGAAT
ENST00000690008.1:c.*62+38_*62+39insATAAAGAAT	ENSP00000508938.1:n.*62+38_*62+39insATAAAGAAT
ENST00000692075.1:n.468+38_468+39insATAAAGAAT
ENST00000692168.1:n.391+38_391+39insATAAAGAAT
ENST00000692416.1:c.66+38_66+39insATAAAGAAT	ENSP00000509527.1:n.66+38_66+39insATAAAGAAT
ENST00000693375.1:c.66+38_66+39insATAAAGAAT	ENSP00000508585.1:n.66+38_66+39insATAAAGAAT
ENST00000693442.1:c.303+38_303+39insATAAAGAAT	ENSP00000509975.1:n.303+38_303+39insATAAAGAAT
ENST00000344442.10:c.303+38_303+39insATAAAGAAT MANE Select	ENSP00000344950.5:n.303+38_303+39insATAAAGAAT
ENST00000651579.1:c.303+38_303+39insATAAAGAAT	ENSP00000499190.1:n.303+38_303+39insATAAAGAAT
ENST00000324052.10:c.303+38_303+39insATAAAGAAT	ENSP00000314311.6:n.303+38_303+39insATAAAGAAT
ENST00000344442.9:c.303+38_303+39insATAAAGAAT	ENSP00000344950.5:n.303+38_303+39insATAAAGAAT
ENST00000505034.5:c.303+38_303+39insATAAAGAAT	ENSP00000421541.1:n.303+38_303+39insATAAAGAAT
ENST00000505216.1:c.*62+38_*62+39insATAAAGAAT	ENSP00000424116.1:n.*62+38_*62+39insATAAAGAAT
ENST00000507443.1:c.303+38_303+39insATAAAGAAT	ENSP00000421963.1:n.303+38_303+39insATAAAGAAT
ENST00000508577.5:c.303+38_303+39insATAAAGAAT	ENSP00000426646.1:n.303+38_303+39insATAAAGAAT
ENST00000509061.5:c.324+38_324+39insATAAAGAAT	ENSP00000422626.1:n.324+38_324+39insATAAAGAAT
ENST00000509622.5:c.*62+38_*62+39insATAAAGAAT	ENSP00000422451.1:n.*62+38_*62+39insATAAAGAAT
ENST00000512589.5:c.*109+38_*109+39insATAAAGAAT	ENSP00000426709.1:n.*109+38_*109+39insATAAAGAAT
ENST00000513553.5:c.31-1230_31-1229insATAAAGAAT	ENSP00000422013.1:n.31-1230_31-1229insATAAAGAAT
NM_001267039.1:c.324+38_324+39insATAAAGAAT	NP_001253968.1:n.324+38_324+39insATAAAGAAT
NM_015454.2:c.303+38_303+39insATAAAGAAT	NP_056269.1:n.303+38_303+39insATAAAGAAT
NM_016648.3:c.303+38_303+39insATAAAGAAT	NP_057732.2:n.303+38_303+39insATAAAGAAT
NR_049768.1:n.478+38_478+39insATAAAGAAT
XM_024454080.1:c.303+38_303+39insATAAAGAAT	XP_024309848.1:n.303+38_303+39insATAAAGAAT
XM_024454081.1:c.303+38_303+39insATAAAGAAT	XP_024309849.1:n.303+38_303+39insATAAAGAAT
XM_024454082.1:c.303+38_303+39insATAAAGAAT	XP_024309850.1:n.303+38_303+39insATAAAGAAT
XM_024454083.1:c.303+38_303+39insATAAAGAAT	XP_024309851.1:n.303+38_303+39insATAAAGAAT
XM_024454084.1:c.303+38_303+39insATAAAGAAT	XP_024309852.1:n.303+38_303+39insATAAAGAAT
XM_024454085.1:c.303+38_303+39insATAAAGAAT	XP_024309853.1:n.303+38_303+39insATAAAGAAT
XM_024454086.1:c.66+38_66+39insATAAAGAAT	XP_024309854.1:n.66+38_66+39insATAAAGAAT
XM_024454087.1:c.66+38_66+39insATAAAGAAT	XP_024309855.1:n.66+38_66+39insATAAAGAAT
XM_024454088.1:c.66+38_66+39insATAAAGAAT	XP_024309856.1:n.66+38_66+39insATAAAGAAT
XM_024454089.1:c.-596_-595insATAAAGAAT	XP_024309857.1:n.-596_-595insATAAAGAAT
NM_016648.4:c.303+38_303+39insATAAAGAAT MANE Select	NP_057732.2:n.303+38_303+39insATAAAGAAT
NM_001370974.1:c.303+38_303+39insATAAAGAAT	NP_001357903.1:n.303+38_303+39insATAAAGAAT
NM_001370975.1:c.303+38_303+39insATAAAGAAT	NP_001357904.1:n.303+38_303+39insATAAAGAAT
NM_001370976.1:c.303+38_303+39insATAAAGAAT	NP_001357905.1:n.303+38_303+39insATAAAGAAT
NM_001370977.1:c.303+38_303+39insATAAAGAAT	NP_001357906.1:n.303+38_303+39insATAAAGAAT
NM_001370978.1:c.303+38_303+39insATAAAGAAT	NP_001357907.1:n.303+38_303+39insATAAAGAAT
NM_001370979.1:c.303+38_303+39insATAAAGAAT	NP_001357908.1:n.303+38_303+39insATAAAGAAT
NM_001370980.1:c.303+38_303+39insATAAAGAAT	NP_001357909.1:n.303+38_303+39insATAAAGAAT
NM_001370981.1:c.66+38_66+39insATAAAGAAT	NP_001357910.1:n.66+38_66+39insATAAAGAAT
NM_001370982.1:c.66+38_66+39insATAAAGAAT	NP_001357911.1:n.66+38_66+39insATAAAGAAT
NM_001267039.2:c.324+38_324+39insATAAAGAAT	NP_001253968.1:n.324+38_324+39insATAAAGAAT
NM_015454.3:c.303+38_303+39insATAAAGAAT	NP_056269.1:n.303+38_303+39insATAAAGAAT
NM_001267039.4:c.303+38_303+39insATAAAGAAT	NP_001253968.2:n.303+38_303+39insATAAAGAAT