Canonical Allele Identifier: CA1266824936

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551942C= , CM000664.2:g.85551942C=	GRCh38
NC_000002.11:g.85779065C= , CM000664.1:g.85779065C=	GRCh37
NC_000002.10:g.85632576C=	NCBI36
NG_011811.2:g.14593G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5957G=
ENST00000482662.2:n.4364G=
ENST00000685865.1:n.2316G=
ENST00000687250.1:n.2016G=
ENST00000687995.1:n.1831G=
ENST00000688205.1:c.*1072G=	ENSP00000509673.1:n.*1072G=
ENST00000688788.1:n.1718G=
ENST00000689276.1:c.1410G=	ENSP00000510012.1:p.Trp470=
ENST00000689576.1:c.*98G=	ENSP00000508712.1:n.*98G=
ENST00000690108.1:c.*1135G=	ENSP00000510617.1:n.*1135G=
ENST00000690468.1:c.*31G=	ENSP00000509078.1:n.*31G=
ENST00000690595.1:c.804G=	ENSP00000508979.1:p.Trp268=
ENST00000691348.1:c.*31G=	ENSP00000509369.1:n.*31G=
ENST00000691410.1:c.*1056G=	ENSP00000508479.1:n.*1056G=
ENST00000693287.1:c.795G=	ENSP00000510264.1:p.Trp265=
ENST00000693681.1:c.792G=	ENSP00000510789.1:p.Trp264=
ENST00000233838.9:c.1479G= MANE Select	ENSP00000233838.3:p.Trp493=
ENST00000233838.8:c.1479G=	ENSP00000233838.3:p.Trp493=
ENST00000430215.7:c.1308G=	ENSP00000408045.3:p.Trp436=
ENST00000465637.5:n.179-3938G=
NM_000821.5:c.1479G=	NP_000812.2:p.Trp493=
NM_000821.6:c.1479G=	NP_000812.2:p.Trp493=
NM_001142269.2:c.1308G=	NP_001135741.1:p.Trp436=
NM_001142269.3:c.1308G=	NP_001135741.1:p.Trp436=
XM_005264259.3:c.1479G=	XP_005264316.1:p.Trp493=
XM_011532764.1:c.657G=	XP_011531066.1:p.Trp219=
XM_011532765.1:c.657G=	XP_011531067.1:p.Trp219=
XR_939677.1:n.1392G=
XM_005264259.5:c.1479G=	XP_005264316.1:p.Trp493=
XM_011532764.3:c.657G=	XP_011531066.1:p.Trp219=
XM_011532765.3:c.657G=	XP_011531067.1:p.Trp219=
XM_017003803.2:c.1308G=	XP_016859292.1:p.Trp436=
XR_001738703.2:n.1392G=
NM_000821.7:c.1479G= MANE Select	NP_000812.2:p.Trp493=
NM_001142269.4:c.1308G=	NP_001135741.1:p.Trp436=