Canonical Allele Identifier: CA1266825385

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85552996G= , CM000664.2:g.85552996G=	GRCh38
NC_000002.11:g.85780119G= , CM000664.1:g.85780119G=	GRCh37
NC_000002.10:g.85633630G=	NCBI36
NG_011811.2:g.13539C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5274C=
ENST00000482662.2:n.3681C=
ENST00000685865.1:n.1633C=
ENST00000687250.1:n.1333C=
ENST00000687995.1:n.1582C=
ENST00000688205.1:c.*823C=	ENSP00000509673.1:n.*823C=
ENST00000688788.1:n.1469C=
ENST00000689276.1:c.1161C=	ENSP00000510012.1:p.His387=
ENST00000689576.1:c.1230C=	ENSP00000508712.1:p.His410=
ENST00000690108.1:c.*886C=	ENSP00000510617.1:n.*886C=
ENST00000690468.1:c.951C=	ENSP00000509078.1:p.His317=
ENST00000690595.1:c.555C=	ENSP00000508979.1:p.His185=
ENST00000691348.1:c.1059C=	ENSP00000509369.1:p.His353=
ENST00000691410.1:c.*807C=	ENSP00000508479.1:n.*807C=
ENST00000693287.1:c.546C=	ENSP00000510264.1:p.His182=
ENST00000693681.1:c.543C=	ENSP00000510789.1:p.His181=
ENST00000233838.9:c.1230C= MANE Select	ENSP00000233838.3:p.His410=
ENST00000233838.8:c.1230C=	ENSP00000233838.3:p.His410=
ENST00000430215.7:c.1059C=	ENSP00000408045.3:p.His353=
ENST00000465637.5:n.179-4992C=
ENST00000473665.1:n.723C=
ENST00000482662.1:n.647C=
NM_000821.5:c.1230C=	NP_000812.2:p.His410=
NM_000821.6:c.1230C=	NP_000812.2:p.His410=
NM_001142269.2:c.1059C=	NP_001135741.1:p.His353=
NM_001142269.3:c.1059C=	NP_001135741.1:p.His353=
XM_005264259.3:c.1230C=	XP_005264316.1:p.His410=
XM_011532764.1:c.408C=	XP_011531066.1:p.His136=
XM_011532765.1:c.408C=	XP_011531067.1:p.His136=
XR_939677.1:n.1295C=
XM_005264259.5:c.1230C=	XP_005264316.1:p.His410=
XM_011532764.3:c.408C=	XP_011531066.1:p.His136=
XM_011532765.3:c.408C=	XP_011531067.1:p.His136=
XM_017003803.2:c.1059C=	XP_016859292.1:p.His353=
XR_001738703.2:n.1295C=
NM_000821.7:c.1230C= MANE Select	NP_000812.2:p.His410=
NM_001142269.4:c.1059C=	NP_001135741.1:p.His353=