Canonical Allele Identifier: CA7565754

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52141200C>T , CM000677.2:g.52141200C>T	GRCh38
NC_000015.9:g.52433397C>T , CM000677.1:g.52433397C>T	GRCh37
NC_000015.8:g.50220689C>T	NCBI36
NG_052868.1:g.55169G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261837.12:c.567G>A MANE Select	ENSP00000261837.7:p.Lys189=
ENST00000261837.11:c.567G>A	ENSP00000261837.7:p.Lys189=
ENST00000358784.11:c.441G>A	ENSP00000351635.7:p.Lys147=
ENST00000396335.8:c.292-5444G>A	ENSP00000379626.4:n.292-5444G>A
ENST00000558519.5:c.12G>A	ENSP00000453339.1:p.Lys4=
ENST00000561313.5:c.*61G>A	ENSP00000454185.1:n.*61G>A
NM_006578.3:c.441G>A	NP_006569.1:p.Lys147=
NM_016194.3:c.567G>A	NP_057278.2:p.Lys189=
XM_011521162.1:c.441G>A	XP_011519464.1:p.Lys147=
XM_011521163.1:c.285G>A	XP_011519465.1:p.Lys95=
XM_011521162.3:c.441G>A	XP_011519464.1:p.Lys147=
XM_011521163.3:c.285G>A	XP_011519465.1:p.Lys95=
XM_017021867.2:c.18G>A	XP_016877356.1:p.Lys6=
XR_001751060.2:n.519G>A
NM_006578.4:c.441G>A	NP_006569.1:p.Lys147=
NM_016194.4:c.567G>A MANE Select	NP_057278.2:p.Lys189=
NM_001379343.1:c.285G>A	NP_001366272.1:p.Lys95=