Canonical Allele Identifier: CA15212365
Gene: ITGA4 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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