Canonical Allele Identifier: CA1266824946

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551966A= , CM000664.2:g.85551966A=	GRCh38
NC_000002.11:g.85779089A= , CM000664.1:g.85779089A=	GRCh37
NC_000002.10:g.85632600A=	NCBI36
NG_011811.2:g.14569T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5933T=
ENST00000482662.2:n.4340T=
ENST00000685865.1:n.2292T=
ENST00000687250.1:n.1992T=
ENST00000687995.1:n.1807T=
ENST00000688205.1:c.*1048T=	ENSP00000509673.1:n.*1048T=
ENST00000688788.1:n.1694T=
ENST00000689276.1:c.1386T=	ENSP00000510012.1:p.Arg462=
ENST00000689576.1:c.*74T=	ENSP00000508712.1:n.*74T=
ENST00000690108.1:c.*1111T=	ENSP00000510617.1:n.*1111T=
ENST00000690468.1:c.*7T=	ENSP00000509078.1:n.*7T=
ENST00000690595.1:c.780T=	ENSP00000508979.1:p.Arg260=
ENST00000691348.1:c.*7T=	ENSP00000509369.1:n.*7T=
ENST00000691410.1:c.*1032T=	ENSP00000508479.1:n.*1032T=
ENST00000693287.1:c.771T=	ENSP00000510264.1:p.Arg257=
ENST00000693681.1:c.768T=	ENSP00000510789.1:p.Arg256=
ENST00000233838.9:c.1455T= MANE Select	ENSP00000233838.3:p.Arg485=
ENST00000233838.8:c.1455T=	ENSP00000233838.3:p.Arg485=
ENST00000430215.7:c.1284T=	ENSP00000408045.3:p.Arg428=
ENST00000465637.5:n.179-3962T=
NM_000821.5:c.1455T=	NP_000812.2:p.Arg485=
NM_000821.6:c.1455T=	NP_000812.2:p.Arg485=
NM_001142269.2:c.1284T=	NP_001135741.1:p.Arg428=
NM_001142269.3:c.1284T=	NP_001135741.1:p.Arg428=
XM_005264259.3:c.1455T=	XP_005264316.1:p.Arg485=
XM_011532764.1:c.633T=	XP_011531066.1:p.Arg211=
XM_011532765.1:c.633T=	XP_011531067.1:p.Arg211=
XR_939677.1:n.1368T=
XM_005264259.5:c.1455T=	XP_005264316.1:p.Arg485=
XM_011532764.3:c.633T=	XP_011531066.1:p.Arg211=
XM_011532765.3:c.633T=	XP_011531067.1:p.Arg211=
XM_017003803.2:c.1284T=	XP_016859292.1:p.Arg428=
XR_001738703.2:n.1368T=
NM_000821.7:c.1455T= MANE Select	NP_000812.2:p.Arg485=
NM_001142269.4:c.1284T=	NP_001135741.1:p.Arg428=