Canonical Allele Identifier: CA2261365378

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374718_44374719delinsTG , CM000679.2:g.44374718_44374719delinsTG	GRCh38
NC_000017.10:g.42452086_42452087delinsTG , CM000679.1:g.42452086_42452087delinsTG	GRCh37
NC_000017.9:g.39807612_39807613delinsTG	NCBI36
NG_008331.1:g.19787_19788delinsCA , LRG_479:g.19787_19788delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2883_2884delinsCA MANE Select	ENSP00000262407.5:p.Phe961=
ENST00000648408.1:c.2314_2315delinsCA
ENST00000262407.5:c.2883_2884delinsCA	ENSP00000262407.5:p.Phe961=
ENST00000587295.5:c.253+1114_253+1115delinsCA
ENST00000592462.5:n.2394_2395delinsCA
NM_000419.3:c.2883_2884delinsCA , LRG_479t1:c.2883_2884delinsCA	NP_000410.2:p.Phe961=
XM_011524749.1:c.2842-249_2842-248delinsCA	XP_011523051.1:n.2842-249_2842-248delinsCA
XM_011524750.1:c.2883_2884delinsCA	XP_011523052.1:p.Phe961=
NM_000419.4:c.2883_2884delinsCA	NP_000410.2:p.Phe961=
NM_000419.5:c.2883_2884delinsCA MANE Select	NP_000410.2:p.Phe961=