Canonical Allele Identifier: CA270675997

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52123049_52123050insTA , CM000677.2:g.52123049_52123050insTA	GRCh38
NC_000015.9:g.52415246_52415247insTA , CM000677.1:g.52415246_52415247insTA	GRCh37
NC_000015.8:g.50202538_50202539insTA	NCBI36
NG_052868.1:g.73319_73320insTA

Transcript Alleles

HGVS	Amino-acid Change
NM_016194.4:c.1177-282_1177-281insTA MANE Select	NP_057278.2:n.1177-282_1177-281insTA
ENST00000261837.12:c.1177-282_1177-281insTA MANE Select	ENSP00000261837.7:n.1177-282_1177-281insTA
NM_001379343.1:c.895-282_895-281insTA	NP_001366272.1:n.895-282_895-281insTA
NM_006578.3:c.1051-282_1051-281insTA	NP_006569.1:n.1051-282_1051-281insTA
NM_006578.4:c.1051-282_1051-281insTA	NP_006569.1:n.1051-282_1051-281insTA
NM_016194.3:c.1177-282_1177-281insTA	NP_057278.2:n.1177-282_1177-281insTA
ENST00000261837.11:c.1177-282_1177-281insTA	ENSP00000261837.7:n.1177-282_1177-281insTA
ENST00000358784.11:c.1051-282_1051-281insTA	ENSP00000351635.7:n.1051-282_1051-281insTA
ENST00000396335.8:c.841-282_841-281insTA	ENSP00000379626.4:n.841-282_841-281insTA
ENST00000557936.5:n.865-282_865-281insTA
ENST00000559348.5:n.1658-282_1658-281insTA
XM_011521162.1:c.1051-282_1051-281insTA	XP_011519464.1:n.1051-282_1051-281insTA
XM_011521162.3:c.1051-282_1051-281insTA	XP_011519464.1:n.1051-282_1051-281insTA
XM_011521163.1:c.895-282_895-281insTA	XP_011519465.1:n.895-282_895-281insTA
XM_011521163.3:c.895-282_895-281insTA	XP_011519465.1:n.895-282_895-281insTA
XM_017021867.2:c.628-282_628-281insTA	XP_016877356.1:n.628-282_628-281insTA
XR_001751060.2:n.1129-282_1129-281insTA