Canonical Allele Identifier: CA1358122966
Gene: ITGA9 HGNC NCBI

Linked Data

dbSNP Id: rs1256407536

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562466_37562467del , CM000665.2:g.37562466_37562467del GRCh38
NC_000003.11:g.37603957_37603958del , CM000665.1:g.37603957_37603958del GRCh37
NC_000003.10:g.37578961_37578962del NCBI36
NG_016166.1:g.115145_115146del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19881_1689+19882del MANE Select ENSP00000264741.5:n.1689+19881_1689+19882del
ENST00000264741.9:c.1689+19881_1689+19882del ENSP00000264741.5:n.1689+19881_1689+19882del
ENST00000422441.5:c.1689+19881_1689+19882del ENSP00000397258.1:n.1689+19881_1689+19882del
NM_002207.2:c.1689+19881_1689+19882del NP_002198.2:n.1689+19881_1689+19882del
NM_002207.3:c.1689+19881_1689+19882del MANE Select NP_002198.2:n.1689+19881_1689+19882del