Canonical Allele Identifier: CA1358123011

Gene: ITGA9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37562557C= , CM000665.2:g.37562557C=	GRCh38
NC_000003.11:g.37604048C= , CM000665.1:g.37604048C=	GRCh37
NC_000003.10:g.37579052C=	NCBI36
NG_016166.1:g.115236C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264741.10:c.1689+19972C= MANE Select	ENSP00000264741.5:n.1689+19972C=
ENST00000264741.9:c.1689+19972C=	ENSP00000264741.5:n.1689+19972C=
ENST00000422441.5:c.1689+19972C=	ENSP00000397258.1:n.1689+19972C=
NM_002207.2:c.1689+19972C=	NP_002198.2:n.1689+19972C=
NM_002207.3:c.1689+19972C= MANE Select	NP_002198.2:n.1689+19972C=