Canonical Allele Identifier: CA357921773

Gene: LARP7

Linked Data

• gnomAD v4: 4-112646447-T-C
• MyVariant Identifiers: chr4:g.113567603T>C (hg19) ; chr4:g.112646447T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.112646447T>C , CM000666.2:g.112646447T>C	GRCh38
NC_000004.11:g.113567603T>C , CM000666.1:g.113567603T>C	GRCh37
NC_000004.10:g.113787052T>C	NCBI36
NG_032779.1:g.14484T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505034.6:c.299T>C	ENSP00000421541.2:p.Val100Ala
ENST00000505216.2:c.*58T>C	ENSP00000424116.1:n.*58T>C
ENST00000694891.1:c.299T>C	ENSP00000511571.1:p.Val100Ala
ENST00000694892.1:n.303T>C
ENST00000694893.1:n.392T>C
ENST00000694894.1:c.299T>C	ENSP00000511572.1:p.Val100Ala
ENST00000694895.1:c.299T>C	ENSP00000511573.1:p.Val100Ala
ENST00000694896.1:c.299T>C	ENSP00000511574.1:p.Val100Ala
ENST00000694897.1:c.299T>C	ENSP00000511575.1:p.Val100Ala
ENST00000694898.1:c.299T>C	ENSP00000511576.1:p.Val100Ala
ENST00000694899.1:c.299T>C	ENSP00000511577.1:p.Val100Ala
ENST00000694900.1:c.299T>C	ENSP00000511578.1:p.Val100Ala
ENST00000694901.1:c.*58T>C	ENSP00000511579.1:n.*58T>C
ENST00000694902.1:n.820T>C
ENST00000511529.2:c.299T>C	ENSP00000426376.2:p.Val100Ala
ENST00000512361.2:n.408T>C
ENST00000512589.6:c.*105T>C	ENSP00000426709.1:n.*105T>C
ENST00000684864.1:c.299T>C	ENSP00000509993.1:p.Val100Ala
ENST00000688617.1:n.573T>C
ENST00000689262.1:n.1450T>C
ENST00000689844.1:c.299T>C	ENSP00000509899.1:p.Val100Ala
ENST00000690008.1:c.*58T>C	ENSP00000508938.1:n.*58T>C
ENST00000692075.1:n.464T>C
ENST00000692168.1:n.387T>C
ENST00000692416.1:c.62T>C	ENSP00000509527.1:p.Val21Ala
ENST00000693375.1:c.62T>C	ENSP00000508585.1:p.Val21Ala
ENST00000693442.1:c.299T>C	ENSP00000509975.1:p.Val100Ala
ENST00000344442.10:c.299T>C MANE Select	ENSP00000344950.5:p.Val100Ala
ENST00000651579.1:c.299T>C	ENSP00000499190.1:p.Val100Ala
ENST00000324052.10:c.299T>C	ENSP00000314311.6:p.Val100Ala
ENST00000344442.9:c.299T>C	ENSP00000344950.5:p.Val100Ala
ENST00000505034.5:c.299T>C	ENSP00000421541.1:p.Val100Ala
ENST00000505216.1:c.*58T>C	ENSP00000424116.1:n.*58T>C
ENST00000507443.1:c.299T>C	ENSP00000421963.1:p.Val100Ala
ENST00000508577.5:c.299T>C	ENSP00000426646.1:p.Val100Ala
ENST00000509061.5:c.320T>C	ENSP00000422626.1:p.Val107Ala
ENST00000509622.5:c.*58T>C	ENSP00000422451.1:n.*58T>C
ENST00000512589.5:c.*105T>C	ENSP00000426709.1:n.*105T>C
ENST00000513553.5:c.31-1272T>C	ENSP00000422013.1:n.31-1272T>C
NM_001267039.1:c.320T>C	NP_001253968.1:p.Val107Ala
NM_015454.2:c.299T>C	NP_056269.1:p.Val100Ala
NM_016648.3:c.299T>C	NP_057732.2:p.Val100Ala
NR_049768.1:n.474T>C
XM_024454080.1:c.299T>C	XP_024309848.1:p.Val100Ala
XM_024454081.1:c.299T>C	XP_024309849.1:p.Val100Ala
XM_024454082.1:c.299T>C	XP_024309850.1:p.Val100Ala
XM_024454083.1:c.299T>C	XP_024309851.1:p.Val100Ala
XM_024454084.1:c.299T>C	XP_024309852.1:p.Val100Ala
XM_024454085.1:c.299T>C	XP_024309853.1:p.Val100Ala
XM_024454086.1:c.62T>C	XP_024309854.1:p.Val21Ala
XM_024454087.1:c.62T>C	XP_024309855.1:p.Val21Ala
XM_024454088.1:c.62T>C	XP_024309856.1:p.Val21Ala
XM_024454089.1:c.-638T>C	XP_024309857.1:n.-638T>C
NM_016648.4:c.299T>C MANE Select	NP_057732.2:p.Val100Ala
NM_001370974.1:c.299T>C	NP_001357903.1:p.Val100Ala
NM_001370975.1:c.299T>C	NP_001357904.1:p.Val100Ala
NM_001370976.1:c.299T>C	NP_001357905.1:p.Val100Ala
NM_001370977.1:c.299T>C	NP_001357906.1:p.Val100Ala
NM_001370978.1:c.299T>C	NP_001357907.1:p.Val100Ala
NM_001370979.1:c.299T>C	NP_001357908.1:p.Val100Ala
NM_001370980.1:c.299T>C	NP_001357909.1:p.Val100Ala
NM_001370981.1:c.62T>C	NP_001357910.1:p.Val21Ala
NM_001370982.1:c.62T>C	NP_001357911.1:p.Val21Ala
NM_001267039.2:c.320T>C	NP_001253968.1:p.Val107Ala
NM_015454.3:c.299T>C	NP_056269.1:p.Val100Ala
NM_001267039.4:c.299T>C	NP_001253968.2:p.Val100Ala