Canonical Allele Identifier: CA14160332

Gene: GNB5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.52125858G>A , CM000677.2:g.52125858G>A	GRCh38
NC_000015.9:g.52418055G>A , CM000677.1:g.52418055G>A	GRCh37
NC_000015.8:g.50205347G>A	NCBI36
NG_052868.1:g.70511C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016194.4:c.1009+90C>T MANE Select	NP_057278.2:n.1009+90C>T
ENST00000261837.12:c.1009+90C>T MANE Select	ENSP00000261837.7:n.1009+90C>T
NM_001379343.1:c.727+90C>T	NP_001366272.1:n.727+90C>T
NM_006578.3:c.883+90C>T	NP_006569.1:n.883+90C>T
NM_006578.4:c.883+90C>T	NP_006569.1:n.883+90C>T
NM_016194.3:c.1009+90C>T	NP_057278.2:n.1009+90C>T
ENST00000261837.11:c.1009+90C>T	ENSP00000261837.7:n.1009+90C>T
ENST00000358784.11:c.883+90C>T	ENSP00000351635.7:n.883+90C>T
ENST00000396335.8:c.673+90C>T	ENSP00000379626.4:n.673+90C>T
ENST00000557936.5:n.697+90C>T
ENST00000558519.5:c.506+90C>T	ENSP00000453339.1:n.506+90C>T
ENST00000559348.5:n.1490+90C>T
ENST00000559541.1:n.473+90C>T
ENST00000560085.1:n.265C>T
XM_011521162.1:c.883+90C>T	XP_011519464.1:n.883+90C>T
XM_011521162.3:c.883+90C>T	XP_011519464.1:n.883+90C>T
XM_011521163.1:c.727+90C>T	XP_011519465.1:n.727+90C>T
XM_011521163.3:c.727+90C>T	XP_011519465.1:n.727+90C>T
XM_017021867.2:c.460+90C>T	XP_016877356.1:n.460+90C>T
XR_001751060.2:n.961+90C>T