Canonical Allele Identifier: CA2628513919

Gene: GNB5

Linked Data

• gnomAD v4: 15-52153975-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52153977del , CM000677.2:g.52153977del	GRCh38
NC_000015.9:g.52446174del , CM000677.1:g.52446174del	GRCh37
NC_000015.8:g.50233466del	NCBI36
NG_052868.1:g.42393del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261837.12:c.339del MANE Select	ENSP00000261837.7:p.Trp113CysfsTer9
ENST00000261837.11:c.339del	ENSP00000261837.7:p.Trp113CysfsTer9
ENST00000358784.11:c.213del	ENSP00000351635.7:p.Trp71CysfsTer9
ENST00000396335.8:c.213del	ENSP00000379626.4:p.Trp71CysfsTer9
ENST00000560075.1:n.370del
ENST00000560116.1:c.213del	ENSP00000453176.1:p.Trp71CysfsTer9
ENST00000561313.5:c.213del	ENSP00000454185.1:p.Trp71CysfsTer9
NM_006578.3:c.213del	NP_006569.1:p.Trp71CysfsTer9
NM_016194.3:c.339del	NP_057278.2:p.Trp113CysfsTer9
XM_011521162.1:c.213del	XP_011519464.1:p.Trp71CysfsTer9
XM_011521163.1:c.57del	XP_011519465.1:p.Trp19CysfsTer9
XM_011521162.3:c.213del	XP_011519464.1:p.Trp71CysfsTer9
XM_011521163.3:c.57del	XP_011519465.1:p.Trp19CysfsTer9
XR_001751060.2:n.291del
NM_006578.4:c.213del	NP_006569.1:p.Trp71CysfsTer9
NM_016194.4:c.339del MANE Select	NP_057278.2:p.Trp113CysfsTer9
NM_001379343.1:c.57del	NP_001366272.1:p.Trp19CysfsTer9