Canonical Allele Identifier: CA7565591

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52128197G>T , CM000677.2:g.52128197G>T	GRCh38
NC_000015.9:g.52420394G>T , CM000677.1:g.52420394G>T	GRCh37
NC_000015.8:g.50207686G>T	NCBI36
NG_052868.1:g.68172C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.911C>A MANE Select	ENSP00000261837.7:p.Thr304Lys
ENST00000261837.11:c.911C>A	ENSP00000261837.7:p.Thr304Lys
ENST00000358784.11:c.785C>A	ENSP00000351635.7:p.Thr262Lys
ENST00000396335.8:c.575C>A	ENSP00000379626.4:p.Thr192Lys
ENST00000557936.5:n.599C>A
ENST00000558519.5:c.408C>A	ENSP00000453339.1:n.408C>A
ENST00000559348.5:n.1392C>A
ENST00000559541.1:n.375C>A
ENST00000560085.1:n.77C>A
NM_006578.3:c.785C>A	NP_006569.1:p.Thr262Lys
NM_016194.3:c.911C>A	NP_057278.2:p.Thr304Lys
XM_011521162.1:c.785C>A	XP_011519464.1:p.Thr262Lys
XM_011521163.1:c.629C>A	XP_011519465.1:p.Thr210Lys
XM_011521162.3:c.785C>A	XP_011519464.1:p.Thr262Lys
XM_011521163.3:c.629C>A	XP_011519465.1:p.Thr210Lys
XM_017021867.2:c.362C>A	XP_016877356.1:p.Thr121Lys
XR_001751060.2:n.863C>A
NM_006578.4:c.785C>A	NP_006569.1:p.Thr262Lys
NM_016194.4:c.911C>A MANE Select	NP_057278.2:p.Thr304Lys
NM_001379343.1:c.629C>A	NP_001366272.1:p.Thr210Lys