Canonical Allele Identifier: CA1358122958

Gene: ITGA9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37562447T= , CM000665.2:g.37562447T=	GRCh38
NC_000003.11:g.37603938T= , CM000665.1:g.37603938T=	GRCh37
NC_000003.10:g.37578942T=	NCBI36
NG_016166.1:g.115126T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264741.10:c.1689+19862T= MANE Select	ENSP00000264741.5:n.1689+19862T=
ENST00000264741.9:c.1689+19862T=	ENSP00000264741.5:n.1689+19862T=
ENST00000422441.5:c.1689+19862T=	ENSP00000397258.1:n.1689+19862T=
NM_002207.2:c.1689+19862T=	NP_002198.2:n.1689+19862T=
NM_002207.3:c.1689+19862T= MANE Select	NP_002198.2:n.1689+19862T=