Canonical Allele Identifier: CA1266825501

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553236G= , CM000664.2:g.85553236G=	GRCh38
NC_000002.11:g.85780359G= , CM000664.1:g.85780359G=	GRCh37
NC_000002.10:g.85633870G=	NCBI36
NG_011811.2:g.13299C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5195C=
ENST00000482662.2:n.3602C=
ENST00000685865.1:n.1554C=
ENST00000687250.1:n.1254C=
ENST00000687995.1:n.1503C=
ENST00000688205.1:c.*744C=	ENSP00000509673.1:n.*744C=
ENST00000688788.1:n.1390C=
ENST00000689276.1:c.1082C=	ENSP00000510012.1:p.Thr361=
ENST00000689576.1:c.1151C=	ENSP00000508712.1:p.Thr384=
ENST00000690108.1:c.*807C=	ENSP00000510617.1:n.*807C=
ENST00000690468.1:c.872C=	ENSP00000509078.1:p.Thr291=
ENST00000690595.1:c.476C=	ENSP00000508979.1:p.Thr159=
ENST00000691348.1:c.980C=	ENSP00000509369.1:p.Thr327=
ENST00000691410.1:c.*728C=	ENSP00000508479.1:n.*728C=
ENST00000693287.1:c.467C=	ENSP00000510264.1:p.Thr156=
ENST00000693681.1:c.464C=	ENSP00000510789.1:p.Thr155=
ENST00000233838.9:c.1151C= MANE Select	ENSP00000233838.3:p.Thr384=
ENST00000233838.8:c.1151C=	ENSP00000233838.3:p.Thr384=
ENST00000430215.7:c.980C=	ENSP00000408045.3:p.Thr327=
ENST00000465637.5:n.179-5232C=
ENST00000473665.1:n.644C=
ENST00000482662.1:n.568C=
NM_000821.5:c.1151C=	NP_000812.2:p.Thr384=
NM_000821.6:c.1151C=	NP_000812.2:p.Thr384=
NM_001142269.2:c.980C=	NP_001135741.1:p.Thr327=
NM_001142269.3:c.980C=	NP_001135741.1:p.Thr327=
XM_005264259.3:c.1151C=	XP_005264316.1:p.Thr384=
XM_011532764.1:c.329C=	XP_011531066.1:p.Thr110=
XM_011532765.1:c.329C=	XP_011531067.1:p.Thr110=
XR_939677.1:n.1216C=
XM_005264259.5:c.1151C=	XP_005264316.1:p.Thr384=
XM_011532764.3:c.329C=	XP_011531066.1:p.Thr110=
XM_011532765.3:c.329C=	XP_011531067.1:p.Thr110=
XM_017003803.2:c.980C=	XP_016859292.1:p.Thr327=
XR_001738703.2:n.1216C=
NM_000821.7:c.1151C= MANE Select	NP_000812.2:p.Thr384=
NM_001142269.4:c.980C=	NP_001135741.1:p.Thr327=