Canonical Allele Identifier: CA1266824917

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551899C= , CM000664.2:g.85551899C=	GRCh38
NC_000002.11:g.85779022C= , CM000664.1:g.85779022C=	GRCh37
NC_000002.10:g.85632533C=	NCBI36
NG_011811.2:g.14636G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6000G=
ENST00000482662.2:n.4407G=
ENST00000685865.1:n.2359G=
ENST00000687250.1:n.2059G=
ENST00000687995.1:n.1874G=
ENST00000688205.1:c.*1115G=	ENSP00000509673.1:n.*1115G=
ENST00000688788.1:n.1761G=
ENST00000689276.1:c.1453G=	ENSP00000510012.1:p.Asp485=
ENST00000689576.1:c.*141G=	ENSP00000508712.1:n.*141G=
ENST00000690108.1:c.*1178G=	ENSP00000510617.1:n.*1178G=
ENST00000690468.1:c.*74G=	ENSP00000509078.1:n.*74G=
ENST00000690595.1:c.847G=	ENSP00000508979.1:p.Asp283=
ENST00000691348.1:c.*74G=	ENSP00000509369.1:n.*74G=
ENST00000691410.1:c.*1099G=	ENSP00000508479.1:n.*1099G=
ENST00000693287.1:c.838G=	ENSP00000510264.1:p.Asp280=
ENST00000693681.1:c.835G=	ENSP00000510789.1:p.Asp279=
ENST00000233838.9:c.1522G= MANE Select	ENSP00000233838.3:p.Asp508=
ENST00000233838.8:c.1522G=	ENSP00000233838.3:p.Asp508=
ENST00000430215.7:c.1351G=	ENSP00000408045.3:p.Asp451=
ENST00000465637.5:n.179-3895G=
NM_000821.5:c.1522G=	NP_000812.2:p.Asp508=
NM_000821.6:c.1522G=	NP_000812.2:p.Asp508=
NM_001142269.2:c.1351G=	NP_001135741.1:p.Asp451=
NM_001142269.3:c.1351G=	NP_001135741.1:p.Asp451=
XM_005264259.3:c.1522G=	XP_005264316.1:p.Asp508=
XM_011532764.1:c.700G=	XP_011531066.1:p.Asp234=
XM_011532765.1:c.700G=	XP_011531067.1:p.Asp234=
XR_939677.1:n.1435G=
XM_005264259.5:c.1522G=	XP_005264316.1:p.Asp508=
XM_011532764.3:c.700G=	XP_011531066.1:p.Asp234=
XM_011532765.3:c.700G=	XP_011531067.1:p.Asp234=
XM_017003803.2:c.1351G=	XP_016859292.1:p.Asp451=
XR_001738703.2:n.1435G=
NM_000821.7:c.1522G= MANE Select	NP_000812.2:p.Asp508=
NM_001142269.4:c.1351G=	NP_001135741.1:p.Asp451=