Canonical Allele Identifier: CA1266825504

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553248G= , CM000664.2:g.85553248G=	GRCh38
NC_000002.11:g.85780371G= , CM000664.1:g.85780371G=	GRCh37
NC_000002.10:g.85633882G=	NCBI36
NG_011811.2:g.13287C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5183C=
ENST00000482662.2:n.3590C=
ENST00000685865.1:n.1542C=
ENST00000687250.1:n.1242C=
ENST00000687995.1:n.1491C=
ENST00000688205.1:c.*732C=	ENSP00000509673.1:n.*732C=
ENST00000688788.1:n.1378C=
ENST00000689276.1:c.1070C=	ENSP00000510012.1:p.Ser357=
ENST00000689576.1:c.1139C=	ENSP00000508712.1:p.Ser380=
ENST00000690108.1:c.*795C=	ENSP00000510617.1:n.*795C=
ENST00000690468.1:c.860C=	ENSP00000509078.1:p.Ser287=
ENST00000690595.1:c.464C=	ENSP00000508979.1:p.Ser155=
ENST00000691348.1:c.968C=	ENSP00000509369.1:p.Ser323=
ENST00000691410.1:c.*716C=	ENSP00000508479.1:n.*716C=
ENST00000693287.1:c.455C=	ENSP00000510264.1:p.Ser152=
ENST00000693681.1:c.452C=	ENSP00000510789.1:p.Ser151=
ENST00000233838.9:c.1139C= MANE Select	ENSP00000233838.3:p.Ser380=
ENST00000233838.8:c.1139C=	ENSP00000233838.3:p.Ser380=
ENST00000430215.7:c.968C=	ENSP00000408045.3:p.Ser323=
ENST00000465637.5:n.179-5244C=
ENST00000473665.1:n.632C=
ENST00000482662.1:n.556C=
NM_000821.5:c.1139C=	NP_000812.2:p.Ser380=
NM_000821.6:c.1139C=	NP_000812.2:p.Ser380=
NM_001142269.2:c.968C=	NP_001135741.1:p.Ser323=
NM_001142269.3:c.968C=	NP_001135741.1:p.Ser323=
XM_005264259.3:c.1139C=	XP_005264316.1:p.Ser380=
XM_011532764.1:c.317C=	XP_011531066.1:p.Ser106=
XM_011532765.1:c.317C=	XP_011531067.1:p.Ser106=
XR_939677.1:n.1204C=
XM_005264259.5:c.1139C=	XP_005264316.1:p.Ser380=
XM_011532764.3:c.317C=	XP_011531066.1:p.Ser106=
XM_011532765.3:c.317C=	XP_011531067.1:p.Ser106=
XM_017003803.2:c.968C=	XP_016859292.1:p.Ser323=
XR_001738703.2:n.1204C=
NM_000821.7:c.1139C= MANE Select	NP_000812.2:p.Ser380=
NM_001142269.4:c.968C=	NP_001135741.1:p.Ser323=