Canonical Allele Identifier: CA2038035993

Gene: ITGA7

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2200C=	ENSP00000452467.1:n.*2200C=
ENST00000554327.6:c.1247C=
ENST00000557058.2:n.1991C=
ENST00000557257.2:c.2102C=	ENSP00000450578.2:p.Ala701=
ENST00000557555.3:c.2588C=	ENSP00000451039.3:p.Ala863=
ENST00000686981.1:c.*2287C=	ENSP00000510795.1:n.*2287C=
ENST00000687390.1:n.682C=
ENST00000691052.1:c.*1060C=	ENSP00000508886.1:n.*1060C=
ENST00000691846.1:c.1389C=
ENST00000691973.1:c.2588C=	ENSP00000509141.1:p.Ala863=
ENST00000257879.11:c.2576C= MANE Select	ENSP00000257879.7:p.Ala859=
ENST00000553804.6:c.2588C=	ENSP00000452120.1:p.Ala863=
ENST00000257879.10:c.2576C=	ENSP00000257879.6:p.Ala859=
ENST00000347027.10:c.2558C=	ENSP00000343009.6:p.Ala853=
ENST00000452168.6:c.2297C=	ENSP00000393844.2:p.Ala766=
ENST00000553804.5:c.2588C=	ENSP00000452120.1:p.Ala863=
ENST00000554327.5:c.641C=
ENST00000555728.5:c.2708C=	ENSP00000452387.1:p.Ala903=
NM_001144996.1:c.2588C=	NP_001138468.1:p.Ala863=
NM_001144997.1:c.2297C=	NP_001138469.1:p.Ala766=
NM_002206.2:c.2576C=	NP_002197.2:p.Ala859=
XM_005268839.1:c.2708C=	XP_005268896.1:p.Ala903=
XM_005268840.1:c.2690C=	XP_005268897.1:p.Ala897=
XM_005268841.1:c.2708C=	XP_005268898.1:p.Ala903=
XM_005268842.1:c.2558C=	XP_005268899.1:p.Ala853=
XM_005268844.1:c.2369C=	XP_005268901.1:p.Ala790=
XM_005268845.1:c.2237C=	XP_005268902.1:p.Ala746=
XM_005268846.1:c.2237C=	XP_005268903.1:p.Ala746=
XM_005268847.1:c.2234C=	XP_005268904.1:p.Ala745=
XM_005268848.1:c.2234C=	XP_005268905.1:p.Ala745=
XM_005268849.1:c.2234C=	XP_005268906.1:p.Ala745=
XM_005268850.1:c.2102C=	XP_005268907.1:p.Ala701=
XM_011538286.1:c.2369C=	XP_011536588.1:p.Ala790=
XM_005268839.2:c.2708C=	XP_005268896.1:p.Ala903=
XM_005268840.2:c.2690C=	XP_005268897.1:p.Ala897=
XM_005268841.2:c.2708C=	XP_005268898.1:p.Ala903=
XM_005268842.2:c.2558C=	XP_005268899.1:p.Ala853=
XM_017019265.1:c.2318C=	XP_016874754.1:p.Ala773=
NM_001144996.2:c.2588C=	NP_001138468.1:p.Ala863=
NM_001367993.1:c.2249C=	NP_001354922.1:p.Ala750=
NM_001367994.1:c.1232C=	NP_001354923.1:p.Ala411=
NM_001374465.1:c.2558C=	NP_001361394.1:p.Ala853=
NM_002206.3:c.2576C= MANE Select	NP_002197.2:p.Ala859=