Canonical Allele Identifier: CA385181760

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087061G>T (hg19) ; chr12:g.55693277G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693277G>T , CM000674.2:g.55693277G>T	GRCh38
NC_000012.11:g.56087061G>T , CM000674.1:g.56087061G>T	GRCh37
NC_000012.10:g.54373328G>T	NCBI36
NG_012343.1:g.24029C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2200C>A	ENSP00000452467.1:n.*2200C>A
ENST00000554327.6:c.1247C>A
ENST00000557058.2:n.1991C>A
ENST00000557257.2:c.2102C>A	ENSP00000450578.2:p.Ala701Asp
ENST00000557555.3:c.2588C>A	ENSP00000451039.3:p.Ala863Asp
ENST00000686981.1:c.*2287C>A	ENSP00000510795.1:n.*2287C>A
ENST00000687390.1:n.682C>A
ENST00000691052.1:c.*1060C>A	ENSP00000508886.1:n.*1060C>A
ENST00000691846.1:c.1389C>A
ENST00000691973.1:c.2588C>A	ENSP00000509141.1:p.Ala863Asp
ENST00000257879.11:c.2576C>A MANE Select	ENSP00000257879.7:p.Ala859Asp
ENST00000553804.6:c.2588C>A	ENSP00000452120.1:p.Ala863Asp
ENST00000257879.10:c.2576C>A	ENSP00000257879.6:p.Ala859Asp
ENST00000347027.10:c.2558C>A	ENSP00000343009.6:p.Ala853Asp
ENST00000452168.6:c.2297C>A	ENSP00000393844.2:p.Ala766Asp
ENST00000553804.5:c.2588C>A	ENSP00000452120.1:p.Ala863Asp
ENST00000554327.5:c.641C>A
ENST00000555728.5:c.2708C>A	ENSP00000452387.1:p.Ala903Asp
NM_001144996.1:c.2588C>A	NP_001138468.1:p.Ala863Asp
NM_001144997.1:c.2297C>A	NP_001138469.1:p.Ala766Asp
NM_002206.2:c.2576C>A	NP_002197.2:p.Ala859Asp
XM_005268839.1:c.2708C>A	XP_005268896.1:p.Ala903Asp
XM_005268840.1:c.2690C>A	XP_005268897.1:p.Ala897Asp
XM_005268841.1:c.2708C>A	XP_005268898.1:p.Ala903Asp
XM_005268842.1:c.2558C>A	XP_005268899.1:p.Ala853Asp
XM_005268844.1:c.2369C>A	XP_005268901.1:p.Ala790Asp
XM_005268845.1:c.2237C>A	XP_005268902.1:p.Ala746Asp
XM_005268846.1:c.2237C>A	XP_005268903.1:p.Ala746Asp
XM_005268847.1:c.2234C>A	XP_005268904.1:p.Ala745Asp
XM_005268848.1:c.2234C>A	XP_005268905.1:p.Ala745Asp
XM_005268849.1:c.2234C>A	XP_005268906.1:p.Ala745Asp
XM_005268850.1:c.2102C>A	XP_005268907.1:p.Ala701Asp
XM_011538286.1:c.2369C>A	XP_011536588.1:p.Ala790Asp
XM_005268839.2:c.2708C>A	XP_005268896.1:p.Ala903Asp
XM_005268840.2:c.2690C>A	XP_005268897.1:p.Ala897Asp
XM_005268841.2:c.2708C>A	XP_005268898.1:p.Ala903Asp
XM_005268842.2:c.2558C>A	XP_005268899.1:p.Ala853Asp
XM_017019265.1:c.2318C>A	XP_016874754.1:p.Ala773Asp
NM_001144996.2:c.2588C>A	NP_001138468.1:p.Ala863Asp
NM_001367993.1:c.2249C>A	NP_001354922.1:p.Ala750Asp
NM_001367994.1:c.1232C>A	NP_001354923.1:p.Ala411Asp
NM_001374465.1:c.2558C>A	NP_001361394.1:p.Ala853Asp
NM_002206.3:c.2576C>A MANE Select	NP_002197.2:p.Ala859Asp