Canonical Allele Identifier: CA1266825503

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553247A= , CM000664.2:g.85553247A=	GRCh38
NC_000002.11:g.85780370A= , CM000664.1:g.85780370A=	GRCh37
NC_000002.10:g.85633881A=	NCBI36
NG_011811.2:g.13288T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5184T=
ENST00000482662.2:n.3591T=
ENST00000685865.1:n.1543T=
ENST00000687250.1:n.1243T=
ENST00000687995.1:n.1492T=
ENST00000688205.1:c.*733T=	ENSP00000509673.1:n.*733T=
ENST00000688788.1:n.1379T=
ENST00000689276.1:c.1071T=	ENSP00000510012.1:p.Ser357=
ENST00000689576.1:c.1140T=	ENSP00000508712.1:p.Ser380=
ENST00000690108.1:c.*796T=	ENSP00000510617.1:n.*796T=
ENST00000690468.1:c.861T=	ENSP00000509078.1:p.Ser287=
ENST00000690595.1:c.465T=	ENSP00000508979.1:p.Ser155=
ENST00000691348.1:c.969T=	ENSP00000509369.1:p.Ser323=
ENST00000691410.1:c.*717T=	ENSP00000508479.1:n.*717T=
ENST00000693287.1:c.456T=	ENSP00000510264.1:p.Ser152=
ENST00000693681.1:c.453T=	ENSP00000510789.1:p.Ser151=
ENST00000233838.9:c.1140T= MANE Select	ENSP00000233838.3:p.Ser380=
ENST00000233838.8:c.1140T=	ENSP00000233838.3:p.Ser380=
ENST00000430215.7:c.969T=	ENSP00000408045.3:p.Ser323=
ENST00000465637.5:n.179-5243T=
ENST00000473665.1:n.633T=
ENST00000482662.1:n.557T=
NM_000821.5:c.1140T=	NP_000812.2:p.Ser380=
NM_000821.6:c.1140T=	NP_000812.2:p.Ser380=
NM_001142269.2:c.969T=	NP_001135741.1:p.Ser323=
NM_001142269.3:c.969T=	NP_001135741.1:p.Ser323=
XM_005264259.3:c.1140T=	XP_005264316.1:p.Ser380=
XM_011532764.1:c.318T=	XP_011531066.1:p.Ser106=
XM_011532765.1:c.318T=	XP_011531067.1:p.Ser106=
XR_939677.1:n.1205T=
XM_005264259.5:c.1140T=	XP_005264316.1:p.Ser380=
XM_011532764.3:c.318T=	XP_011531066.1:p.Ser106=
XM_011532765.3:c.318T=	XP_011531067.1:p.Ser106=
XM_017003803.2:c.969T=	XP_016859292.1:p.Ser323=
XR_001738703.2:n.1205T=
NM_000821.7:c.1140T= MANE Select	NP_000812.2:p.Ser380=
NM_001142269.4:c.969T=	NP_001135741.1:p.Ser323=