Canonical Allele Identifier: CA2038039529

Gene: ITGA7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55695573C= , CM000674.2:g.55695573C=	GRCh38
NC_000012.11:g.56089357C= , CM000674.1:g.56089357C=	GRCh37
NC_000012.10:g.54375624C=	NCBI36
NG_012343.1:g.21733G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002206.3:c.1952G= MANE Select	NP_002197.2:p.Arg651=
ENST00000257879.11:c.1952G= MANE Select	ENSP00000257879.7:p.Arg651=
NM_001144996.1:c.1964G=	NP_001138468.1:p.Arg655=
NM_001144996.2:c.1964G=	NP_001138468.1:p.Arg655=
NM_001144997.1:c.1673G=	NP_001138469.1:p.Arg558=
NM_001367993.1:c.1625G=	NP_001354922.1:p.Arg542=
NM_001367994.1:c.608G=	NP_001354923.1:p.Arg203=
NM_001374465.1:c.1934G=	NP_001361394.1:p.Arg645=
NM_002206.2:c.1952G=	NP_002197.2:p.Arg651=
ENST00000257879.10:c.1952G=	ENSP00000257879.6:p.Arg651=
ENST00000347027.10:c.1934G=	ENSP00000343009.6:p.Arg645=
ENST00000452168.6:c.1673G=	ENSP00000393844.2:p.Arg558=
ENST00000553804.5:c.1964G=	ENSP00000452120.1:p.Arg655=
ENST00000553804.6:c.1964G=	ENSP00000452120.1:p.Arg655=
ENST00000553893.6:c.*1576G=	ENSP00000452467.1:n.*1576G=
ENST00000554327.5:c.210G=
ENST00000554327.6:c.816G=
ENST00000555728.5:c.2084G=	ENSP00000452387.1:p.Arg695=
ENST00000557058.1:n.199G=
ENST00000557058.2:n.816G=
ENST00000557257.2:c.1478G=	ENSP00000450578.2:p.Arg493=
ENST00000557555.3:c.1964G=	ENSP00000451039.3:p.Arg655=
ENST00000686981.1:c.*1663G=	ENSP00000510795.1:n.*1663G=
ENST00000691052.1:c.*436G=	ENSP00000508886.1:n.*436G=
ENST00000691846.1:c.797G=
ENST00000691973.1:c.1964G=	ENSP00000509141.1:p.Arg655=
XM_005268839.1:c.2084G=	XP_005268896.1:p.Arg695=
XM_005268839.2:c.2084G=	XP_005268896.1:p.Arg695=
XM_005268840.1:c.2066G=	XP_005268897.1:p.Arg689=
XM_005268840.2:c.2066G=	XP_005268897.1:p.Arg689=
XM_005268841.1:c.2084G=	XP_005268898.1:p.Arg695=
XM_005268841.2:c.2084G=	XP_005268898.1:p.Arg695=
XM_005268842.1:c.1934G=	XP_005268899.1:p.Arg645=
XM_005268842.2:c.1934G=	XP_005268899.1:p.Arg645=
XM_005268844.1:c.1745G=	XP_005268901.1:p.Arg582=
XM_005268845.1:c.1613G=	XP_005268902.1:p.Arg538=
XM_005268846.1:c.1613G=	XP_005268903.1:p.Arg538=
XM_005268847.1:c.1610G=	XP_005268904.1:p.Arg537=
XM_005268848.1:c.1610G=	XP_005268905.1:p.Arg537=
XM_005268849.1:c.1610G=	XP_005268906.1:p.Arg537=
XM_005268850.1:c.1478G=	XP_005268907.1:p.Arg493=
XM_011538286.1:c.1745G=	XP_011536588.1:p.Arg582=
XM_011538287.1:c.2084G=	XP_011536589.1:p.Arg695=
XM_017019265.1:c.1694G=	XP_016874754.1:p.Arg565=