Canonical Allele Identifier: CA1311878503

Gene: ITGA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181463487G= , CM000664.2:g.181463487G=	GRCh38
NC_000002.11:g.182328214G= , CM000664.1:g.182328214G=	GRCh37
NC_000002.10:g.182036459G=	NCBI36
NG_050623.1:g.11596G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000885.6:c.319+5170G= MANE Select	NP_000876.3:n.319+5170G=
ENST00000397033.7:c.319+5170G= MANE Select	ENSP00000380227.2:n.319+5170G=
NM_000885.4:c.319+5170G=	NP_000876.3:n.319+5170G=
NM_000885.5:c.319+5170G=	NP_000876.3:n.319+5170G=
NM_001316312.1:c.319+5170G=	NP_001303241.1:n.319+5170G=
NM_001316312.2:c.319+5170G=	NP_001303241.1:n.319+5170G=
ENST00000233573.6:c.319+5170G=	ENSP00000233573.6:n.319+5170G=
ENST00000339307.8:c.319+5170G=	ENSP00000340149.4:n.319+5170G=
ENST00000397033.6:c.319+5170G=	ENSP00000380227.2:n.319+5170G=
ENST00000465522.5:n.570+5170G=
ENST00000478440.1:n.77+5170G=
ENST00000484404.1:n.261+5170G=