Canonical Allele Identifier: CA542249064

Gene: ITGA9

Linked Data

• dbSNP Id: rs1291302033
• gnomAD v2: 3-37603929-CCTTTTAGATA-C
• gnomAD v3: 3-37562438-CCTTTTAGATA-C
• gnomAD v4: 3-37562438-CCTTTTAGATA-C
• MyVariant Identifiers: chr3:g.37603930_37603939del (hg19) ; chr3:g.37562439_37562448del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37562444_37562453del , CM000665.2:g.37562444_37562453del	GRCh38
NC_000003.11:g.37603935_37603944del , CM000665.1:g.37603935_37603944del	GRCh37
NC_000003.10:g.37578939_37578948del	NCBI36
NG_016166.1:g.115123_115132del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264741.10:c.1689+19859_1689+19868del MANE Select	ENSP00000264741.5:n.1689+19859_1689+19868del
ENST00000264741.9:c.1689+19859_1689+19868del	ENSP00000264741.5:n.1689+19859_1689+19868del
ENST00000422441.5:c.1689+19859_1689+19868del	ENSP00000397258.1:n.1689+19859_1689+19868del
NM_002207.2:c.1689+19859_1689+19868del	NP_002198.2:n.1689+19859_1689+19868del
NM_002207.3:c.1689+19859_1689+19868del MANE Select	NP_002198.2:n.1689+19859_1689+19868del