Canonical Allele Identifier: CA11588494

Gene: ITGA9

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37548944T>C , CM000665.2:g.37548944T>C	GRCh38
NC_000003.11:g.37590435T>C , CM000665.1:g.37590435T>C	GRCh37
NC_000003.10:g.37565439T>C	NCBI36
NG_016166.1:g.101623T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264741.10:c.1689+6359T>C MANE Select	ENSP00000264741.5:n.1689+6359T>C
ENST00000264741.9:c.1689+6359T>C	ENSP00000264741.5:n.1689+6359T>C
ENST00000422441.5:c.1689+6359T>C	ENSP00000397258.1:n.1689+6359T>C
NM_002207.2:c.1689+6359T>C	NP_002198.2:n.1689+6359T>C
NM_002207.3:c.1689+6359T>C MANE Select	NP_002198.2:n.1689+6359T>C