Canonical Allele Identifier: CA1266824937

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551943C= , CM000664.2:g.85551943C=	GRCh38
NC_000002.11:g.85779066C= , CM000664.1:g.85779066C=	GRCh37
NC_000002.10:g.85632577C=	NCBI36
NG_011811.2:g.14592G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5956G=
ENST00000482662.2:n.4363G=
ENST00000685865.1:n.2315G=
ENST00000687250.1:n.2015G=
ENST00000687995.1:n.1830G=
ENST00000688205.1:c.*1071G=	ENSP00000509673.1:n.*1071G=
ENST00000688788.1:n.1717G=
ENST00000689276.1:c.1409G=	ENSP00000510012.1:p.Trp470=
ENST00000689576.1:c.*97G=	ENSP00000508712.1:n.*97G=
ENST00000690108.1:c.*1134G=	ENSP00000510617.1:n.*1134G=
ENST00000690468.1:c.*30G=	ENSP00000509078.1:n.*30G=
ENST00000690595.1:c.803G=	ENSP00000508979.1:p.Trp268=
ENST00000691348.1:c.*30G=	ENSP00000509369.1:n.*30G=
ENST00000691410.1:c.*1055G=	ENSP00000508479.1:n.*1055G=
ENST00000693287.1:c.794G=	ENSP00000510264.1:p.Trp265=
ENST00000693681.1:c.791G=	ENSP00000510789.1:p.Trp264=
ENST00000233838.9:c.1478G= MANE Select	ENSP00000233838.3:p.Trp493=
ENST00000233838.8:c.1478G=	ENSP00000233838.3:p.Trp493=
ENST00000430215.7:c.1307G=	ENSP00000408045.3:p.Trp436=
ENST00000465637.5:n.179-3939G=
NM_000821.5:c.1478G=	NP_000812.2:p.Trp493=
NM_000821.6:c.1478G=	NP_000812.2:p.Trp493=
NM_001142269.2:c.1307G=	NP_001135741.1:p.Trp436=
NM_001142269.3:c.1307G=	NP_001135741.1:p.Trp436=
XM_005264259.3:c.1478G=	XP_005264316.1:p.Trp493=
XM_011532764.1:c.656G=	XP_011531066.1:p.Trp219=
XM_011532765.1:c.656G=	XP_011531067.1:p.Trp219=
XR_939677.1:n.1391G=
XM_005264259.5:c.1478G=	XP_005264316.1:p.Trp493=
XM_011532764.3:c.656G=	XP_011531066.1:p.Trp219=
XM_011532765.3:c.656G=	XP_011531067.1:p.Trp219=
XM_017003803.2:c.1307G=	XP_016859292.1:p.Trp436=
XR_001738703.2:n.1391G=
NM_000821.7:c.1478G= MANE Select	NP_000812.2:p.Trp493=
NM_001142269.4:c.1307G=	NP_001135741.1:p.Trp436=