Canonical Allele Identifier: CA2638214818

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44374555-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374555_44374556insTG , CM000679.2:g.44374555_44374556insTG	GRCh38
NC_000017.10:g.42451923_42451924insTG , CM000679.1:g.42451923_42451924insTG	GRCh37
NC_000017.9:g.39807449_39807450insTG	NCBI36
NG_008331.1:g.19950_19951insCA , LRG_479:g.19950_19951insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2944-86_2944-85insCA MANE Select	ENSP00000262407.5:n.2944-86_2944-85insCA
ENST00000648408.1:c.2374+103_2374+104insCA
ENST00000262407.5:c.2944-86_2944-85insCA	ENSP00000262407.5:n.2944-86_2944-85insCA
ENST00000587295.5:c.253+1277_253+1278insCA
ENST00000588098.1:c.37+103_37+104insCA
ENST00000592462.5:n.2557_2558insCA
NM_000419.3:c.2944-86_2944-85insCA , LRG_479t1:c.2944-86_2944-85insCA	NP_000410.2:n.2944-86_2944-85insCA
XM_011524749.1:c.2842-86_2842-85insCA	XP_011523051.1:n.2842-86_2842-85insCA
XM_011524750.1:c.2943+103_2943+104insCA	XP_011523052.1:n.2943+103_2943+104insCA
NM_000419.4:c.2944-86_2944-85insCA	NP_000410.2:n.2944-86_2944-85insCA
NM_000419.5:c.2944-86_2944-85insCA MANE Select	NP_000410.2:n.2944-86_2944-85insCA