Canonical Allele Identifier: CA2275653877

Gene: ITGB4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75727778A= , CM000679.2:g.75727778A=	GRCh38
NC_000017.10:g.73723859A= , CM000679.1:g.73723859A=	GRCh37
NC_000017.9:g.71235454A=	NCBI36
NG_007372.1:g.11344A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449880.7:c.392A=	ENSP00000400217.2:p.Asp131=
ENST00000200181.8:c.392A= MANE Select	ENSP00000200181.3:p.Asp131=
ENST00000200181.7:c.392A=	ENSP00000200181.3:p.Asp131=
ENST00000449880.6:c.392A=	ENSP00000400217.2:p.Asp131=
ENST00000450894.7:c.392A=	ENSP00000405536.3:p.Asp131=
ENST00000579662.5:c.392A=	ENSP00000463651.1:p.Asp131=
ENST00000580542.5:n.457A=
ENST00000584558.5:n.392A=
NM_000213.3:c.392A=	NP_000204.3:p.Asp131=
NM_001005619.1:c.392A=	NP_001005619.1:p.Asp131=
NM_001005731.1:c.392A=	NP_001005731.1:p.Asp131=
XM_005257309.2:c.392A=	XP_005257366.1:p.Asp131=
XM_005257311.3:c.392A=	XP_005257368.1:p.Asp131=
XM_005257312.2:c.392A=	XP_005257369.1:p.Asp131=
XM_006721866.2:c.497A=	XP_006721929.1:p.Asp166=
XM_006721867.2:c.497A=	XP_006721930.1:p.Asp166=
XM_006721868.2:c.497A=	XP_006721931.1:p.Asp166=
XM_006721870.2:c.497A=	XP_006721933.1:p.Asp166=
XM_011524751.1:c.497A=	XP_011523053.1:p.Asp166=
NM_000213.4:c.392A=	NP_000204.3:p.Asp131=
NM_001005731.2:c.392A=	NP_001005731.1:p.Asp131=
NM_001321123.1:c.392A=	NP_001308052.1:p.Asp131=
XM_005257311.4:c.392A=	XP_005257368.1:p.Asp131=
XM_006721866.3:c.497A=	XP_006721929.1:p.Asp166=
XM_006721867.3:c.497A=	XP_006721930.1:p.Asp166=
XM_006721868.3:c.497A=	XP_006721931.1:p.Asp166=
XM_006721870.3:c.497A=	XP_006721933.1:p.Asp166=
XM_011524751.2:c.497A=	XP_011523053.1:p.Asp166=
NM_000213.5:c.392A= MANE Select	NP_000204.3:p.Asp131=
NM_001005731.3:c.392A=	NP_001005731.1:p.Asp131=
NM_001321123.2:c.392A=	NP_001308052.1:p.Asp131=