Canonical Allele Identifier: CA1358122955
Gene: ITGA9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562438_37562448delinsCCTTTTAGATA , CM000665.2:g.37562438_37562448delinsCCTTTTAGATA GRCh38
NC_000003.11:g.37603929_37603939delinsCCTTTTAGATA , CM000665.1:g.37603929_37603939delinsCCTTTTAGATA GRCh37
NC_000003.10:g.37578933_37578943delinsCCTTTTAGATA NCBI36
NG_016166.1:g.115117_115127delinsCCTTTTAGATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19853_1689+19863delinsCCTTTTAGATA MANE Select ENSP00000264741.5:n.1689+19853_1689+19863delinsCCTTTTAGATA
ENST00000264741.9:c.1689+19853_1689+19863delinsCCTTTTAGATA ENSP00000264741.5:n.1689+19853_1689+19863delinsCCTTTTAGATA
ENST00000422441.5:c.1689+19853_1689+19863delinsCCTTTTAGATA ENSP00000397258.1:n.1689+19853_1689+19863delinsCCTTTTAGATA
NM_002207.2:c.1689+19853_1689+19863delinsCCTTTTAGATA NP_002198.2:n.1689+19853_1689+19863delinsCCTTTTAGATA
NM_002207.3:c.1689+19853_1689+19863delinsCCTTTTAGATA MANE Select NP_002198.2:n.1689+19853_1689+19863delinsCCTTTTAGATA