Canonical Allele Identifier: CA2177210955

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52153962_52153967delinsCTCTTA , CM000677.2:g.52153962_52153967delinsCTCTTA	GRCh38
NC_000015.9:g.52446159_52446164delinsCTCTTA , CM000677.1:g.52446159_52446164delinsCTCTTA	GRCh37
NC_000015.8:g.50233451_50233456delinsCTCTTA	NCBI36
NG_052868.1:g.42402_42407delinsTAAGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261837.12:c.348_353delinsTAAGAG MANE Select	ENSP00000261837.7:p.Asp116=
ENST00000261837.11:c.348_353delinsTAAGAG	ENSP00000261837.7:p.Asp116=
ENST00000358784.11:c.222_227delinsTAAGAG	ENSP00000351635.7:p.Asp74=
ENST00000396335.8:c.222_227delinsTAAGAG	ENSP00000379626.4:p.Asp74=
ENST00000560075.1:n.379_384delinsTAAGAG
ENST00000560116.1:c.222_227delinsTAAGAG	ENSP00000453176.1:p.Asp74=
ENST00000561313.5:c.222_227delinsTAAGAG	ENSP00000454185.1:p.Asp74=
NM_006578.3:c.222_227delinsTAAGAG	NP_006569.1:p.Asp74=
NM_016194.3:c.348_353delinsTAAGAG	NP_057278.2:p.Asp116=
XM_011521162.1:c.222_227delinsTAAGAG	XP_011519464.1:p.Asp74=
XM_011521163.1:c.66_71delinsTAAGAG	XP_011519465.1:p.Asp22=
XM_011521162.3:c.222_227delinsTAAGAG	XP_011519464.1:p.Asp74=
XM_011521163.3:c.66_71delinsTAAGAG	XP_011519465.1:p.Asp22=
XR_001751060.2:n.300_305delinsTAAGAG
NM_006578.4:c.222_227delinsTAAGAG	NP_006569.1:p.Asp74=
NM_016194.4:c.348_353delinsTAAGAG MANE Select	NP_057278.2:p.Asp116=
NM_001379343.1:c.66_71delinsTAAGAG	NP_001366272.1:p.Asp22=