Canonical Allele Identifier: CA440830344

Gene: LARP7

Linked Data

• MyVariant Identifiers: chr4:g.113567562T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.112646406T>C , CM000666.2:g.112646406T>C	GRCh38
NC_000004.11:g.113567562T>C , CM000666.1:g.113567562T>C	GRCh37
NC_000004.10:g.113787011T>C	NCBI36
NG_032779.1:g.14443T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505034.6:c.258T>C	ENSP00000421541.2:p.Asp86=
ENST00000505216.2:c.*17T>C	ENSP00000424116.1:n.*17T>C
ENST00000694891.1:c.258T>C	ENSP00000511571.1:p.Asp86=
ENST00000694892.1:n.262T>C
ENST00000694893.1:n.351T>C
ENST00000694894.1:c.258T>C	ENSP00000511572.1:p.Asp86=
ENST00000694895.1:c.258T>C	ENSP00000511573.1:p.Asp86=
ENST00000694896.1:c.258T>C	ENSP00000511574.1:p.Asp86=
ENST00000694897.1:c.258T>C	ENSP00000511575.1:p.Asp86=
ENST00000694898.1:c.258T>C	ENSP00000511576.1:p.Asp86=
ENST00000694899.1:c.258T>C	ENSP00000511577.1:p.Asp86=
ENST00000694900.1:c.258T>C	ENSP00000511578.1:p.Asp86=
ENST00000694901.1:c.*17T>C	ENSP00000511579.1:n.*17T>C
ENST00000694902.1:n.779T>C
ENST00000511529.2:c.258T>C	ENSP00000426376.2:p.Asp86=
ENST00000512361.2:n.367T>C
ENST00000512589.6:c.*64T>C	ENSP00000426709.1:n.*64T>C
ENST00000684864.1:c.258T>C	ENSP00000509993.1:p.Asp86=
ENST00000688617.1:n.532T>C
ENST00000689262.1:n.1409T>C
ENST00000689844.1:c.258T>C	ENSP00000509899.1:p.Asp86=
ENST00000690008.1:c.*17T>C	ENSP00000508938.1:n.*17T>C
ENST00000692075.1:n.423T>C
ENST00000692168.1:n.346T>C
ENST00000692416.1:c.21T>C	ENSP00000509527.1:p.Asp7=
ENST00000693375.1:c.21T>C	ENSP00000508585.1:p.Asp7=
ENST00000693442.1:c.258T>C	ENSP00000509975.1:p.Asp86=
ENST00000344442.10:c.258T>C MANE Select	ENSP00000344950.5:p.Asp86=
ENST00000651579.1:c.258T>C	ENSP00000499190.1:p.Asp86=
ENST00000324052.10:c.258T>C	ENSP00000314311.6:p.Asp86=
ENST00000344442.9:c.258T>C	ENSP00000344950.5:p.Asp86=
ENST00000505034.5:c.258T>C	ENSP00000421541.1:p.Asp86=
ENST00000505216.1:c.*17T>C	ENSP00000424116.1:n.*17T>C
ENST00000507443.1:c.258T>C	ENSP00000421963.1:p.Asp86=
ENST00000508577.5:c.258T>C	ENSP00000426646.1:p.Asp86=
ENST00000509061.5:c.279T>C	ENSP00000422626.1:p.Asp93=
ENST00000509622.5:c.*17T>C	ENSP00000422451.1:n.*17T>C
ENST00000512589.5:c.*64T>C	ENSP00000426709.1:n.*64T>C
ENST00000513553.5:c.31-1313T>C	ENSP00000422013.1:n.31-1313T>C
NM_001267039.1:c.279T>C	NP_001253968.1:p.Asp93=
NM_015454.2:c.258T>C	NP_056269.1:p.Asp86=
NM_016648.3:c.258T>C	NP_057732.2:p.Asp86=
NR_049768.1:n.433T>C
XM_024454080.1:c.258T>C	XP_024309848.1:p.Asp86=
XM_024454081.1:c.258T>C	XP_024309849.1:p.Asp86=
XM_024454082.1:c.258T>C	XP_024309850.1:p.Asp86=
XM_024454083.1:c.258T>C	XP_024309851.1:p.Asp86=
XM_024454084.1:c.258T>C	XP_024309852.1:p.Asp86=
XM_024454085.1:c.258T>C	XP_024309853.1:p.Asp86=
XM_024454086.1:c.21T>C	XP_024309854.1:p.Asp7=
XM_024454087.1:c.21T>C	XP_024309855.1:p.Asp7=
XM_024454088.1:c.21T>C	XP_024309856.1:p.Asp7=
XM_024454089.1:c.-679T>C	XP_024309857.1:n.-679T>C
NM_016648.4:c.258T>C MANE Select	NP_057732.2:p.Asp86=
NM_001370974.1:c.258T>C	NP_001357903.1:p.Asp86=
NM_001370975.1:c.258T>C	NP_001357904.1:p.Asp86=
NM_001370976.1:c.258T>C	NP_001357905.1:p.Asp86=
NM_001370977.1:c.258T>C	NP_001357906.1:p.Asp86=
NM_001370978.1:c.258T>C	NP_001357907.1:p.Asp86=
NM_001370979.1:c.258T>C	NP_001357908.1:p.Asp86=
NM_001370980.1:c.258T>C	NP_001357909.1:p.Asp86=
NM_001370981.1:c.21T>C	NP_001357910.1:p.Asp7=
NM_001370982.1:c.21T>C	NP_001357911.1:p.Asp7=
NM_001267039.2:c.279T>C	NP_001253968.1:p.Asp93=
NM_015454.3:c.258T>C	NP_056269.1:p.Asp86=
NM_001267039.4:c.258T>C	NP_001253968.2:p.Asp86=