Canonical Allele Identifier: CA385181747

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56087055A>T (hg19) ; chr12:g.55693271A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693271A>T , CM000674.2:g.55693271A>T	GRCh38
NC_000012.11:g.56087055A>T , CM000674.1:g.56087055A>T	GRCh37
NC_000012.10:g.54373322A>T	NCBI36
NG_012343.1:g.24035T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2206T>A	ENSP00000452467.1:n.*2206T>A
ENST00000554327.6:c.1253T>A
ENST00000557058.2:n.1997T>A
ENST00000557257.2:c.2108T>A	ENSP00000450578.2:p.Leu703His
ENST00000557555.3:c.2594T>A	ENSP00000451039.3:p.Leu865His
ENST00000686981.1:c.*2293T>A	ENSP00000510795.1:n.*2293T>A
ENST00000687390.1:n.688T>A
ENST00000691052.1:c.*1066T>A	ENSP00000508886.1:n.*1066T>A
ENST00000691846.1:c.1395T>A
ENST00000691973.1:c.2594T>A	ENSP00000509141.1:p.Leu865His
ENST00000257879.11:c.2582T>A MANE Select	ENSP00000257879.7:p.Leu861His
ENST00000553804.6:c.2594T>A	ENSP00000452120.1:p.Leu865His
ENST00000257879.10:c.2582T>A	ENSP00000257879.6:p.Leu861His
ENST00000347027.10:c.2564T>A	ENSP00000343009.6:p.Leu855His
ENST00000452168.6:c.2303T>A	ENSP00000393844.2:p.Leu768His
ENST00000553804.5:c.2594T>A	ENSP00000452120.1:p.Leu865His
ENST00000554327.5:c.647T>A
ENST00000555728.5:c.2714T>A	ENSP00000452387.1:p.Leu905His
NM_001144996.1:c.2594T>A	NP_001138468.1:p.Leu865His
NM_001144997.1:c.2303T>A	NP_001138469.1:p.Leu768His
NM_002206.2:c.2582T>A	NP_002197.2:p.Leu861His
XM_005268839.1:c.2714T>A	XP_005268896.1:p.Leu905His
XM_005268840.1:c.2696T>A	XP_005268897.1:p.Leu899His
XM_005268841.1:c.2714T>A	XP_005268898.1:p.Leu905His
XM_005268842.1:c.2564T>A	XP_005268899.1:p.Leu855His
XM_005268844.1:c.2375T>A	XP_005268901.1:p.Leu792His
XM_005268845.1:c.2243T>A	XP_005268902.1:p.Leu748His
XM_005268846.1:c.2243T>A	XP_005268903.1:p.Leu748His
XM_005268847.1:c.2240T>A	XP_005268904.1:p.Leu747His
XM_005268848.1:c.2240T>A	XP_005268905.1:p.Leu747His
XM_005268849.1:c.2240T>A	XP_005268906.1:p.Leu747His
XM_005268850.1:c.2108T>A	XP_005268907.1:p.Leu703His
XM_011538286.1:c.2375T>A	XP_011536588.1:p.Leu792His
XM_005268839.2:c.2714T>A	XP_005268896.1:p.Leu905His
XM_005268840.2:c.2696T>A	XP_005268897.1:p.Leu899His
XM_005268841.2:c.2714T>A	XP_005268898.1:p.Leu905His
XM_005268842.2:c.2564T>A	XP_005268899.1:p.Leu855His
XM_017019265.1:c.2324T>A	XP_016874754.1:p.Leu775His
NM_001144996.2:c.2594T>A	NP_001138468.1:p.Leu865His
NM_001367993.1:c.2255T>A	NP_001354922.1:p.Leu752His
NM_001367994.1:c.1238T>A	NP_001354923.1:p.Leu413His
NM_001374465.1:c.2564T>A	NP_001361394.1:p.Leu855His
NM_002206.3:c.2582T>A MANE Select	NP_002197.2:p.Leu861His