Canonical Allele Identifier: CA1266824911

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551883C= , CM000664.2:g.85551883C=	GRCh38
NC_000002.11:g.85779006C= , CM000664.1:g.85779006C=	GRCh37
NC_000002.10:g.85632517C=	NCBI36
NG_011811.2:g.14652G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6016G=
ENST00000482662.2:n.4423G=
ENST00000685865.1:n.2375G=
ENST00000687250.1:n.2075G=
ENST00000687995.1:n.1890G=
ENST00000688205.1:c.*1131G=	ENSP00000509673.1:n.*1131G=
ENST00000688788.1:n.1777G=
ENST00000689276.1:c.1469G=	ENSP00000510012.1:p.Arg490=
ENST00000689576.1:c.*157G=	ENSP00000508712.1:n.*157G=
ENST00000690108.1:c.*1194G=	ENSP00000510617.1:n.*1194G=
ENST00000690468.1:c.*90G=	ENSP00000509078.1:n.*90G=
ENST00000690595.1:c.863G=	ENSP00000508979.1:p.Arg288=
ENST00000691348.1:c.*90G=	ENSP00000509369.1:n.*90G=
ENST00000691410.1:c.*1115G=	ENSP00000508479.1:n.*1115G=
ENST00000693287.1:c.854G=	ENSP00000510264.1:p.Arg285=
ENST00000693681.1:c.851G=	ENSP00000510789.1:p.Arg284=
ENST00000233838.9:c.1538G= MANE Select	ENSP00000233838.3:p.Arg513=
ENST00000233838.8:c.1538G=	ENSP00000233838.3:p.Arg513=
ENST00000430215.7:c.1367G=	ENSP00000408045.3:p.Arg456=
ENST00000465637.5:n.179-3879G=
NM_000821.5:c.1538G=	NP_000812.2:p.Arg513=
NM_000821.6:c.1538G=	NP_000812.2:p.Arg513=
NM_001142269.2:c.1367G=	NP_001135741.1:p.Arg456=
NM_001142269.3:c.1367G=	NP_001135741.1:p.Arg456=
XM_005264259.3:c.1538G=	XP_005264316.1:p.Arg513=
XM_011532764.1:c.716G=	XP_011531066.1:p.Arg239=
XM_011532765.1:c.716G=	XP_011531067.1:p.Arg239=
XR_939677.1:n.1451G=
XM_005264259.5:c.1538G=	XP_005264316.1:p.Arg513=
XM_011532764.3:c.716G=	XP_011531066.1:p.Arg239=
XM_011532765.3:c.716G=	XP_011531067.1:p.Arg239=
XM_017003803.2:c.1367G=	XP_016859292.1:p.Arg456=
XR_001738703.2:n.1451G=
NM_000821.7:c.1538G= MANE Select	NP_000812.2:p.Arg513=
NM_001142269.4:c.1367G=	NP_001135741.1:p.Arg456=