Canonical Allele Identifier: CA1266824893

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551836C= , CM000664.2:g.85551836C=	GRCh38
NC_000002.11:g.85778959C= , CM000664.1:g.85778959C=	GRCh37
NC_000002.10:g.85632470C=	NCBI36
NG_011811.2:g.14699G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6063G=
ENST00000482662.2:n.4470G=
ENST00000685865.1:n.2422G=
ENST00000687250.1:n.2122G=
ENST00000687995.1:n.1937G=
ENST00000688205.1:c.*1178G=	ENSP00000509673.1:n.*1178G=
ENST00000688788.1:n.1824G=
ENST00000689276.1:c.1516G=	ENSP00000510012.1:p.Val506=
ENST00000689576.1:c.*204G=	ENSP00000508712.1:n.*204G=
ENST00000690108.1:c.*1241G=	ENSP00000510617.1:n.*1241G=
ENST00000690468.1:c.*137G=	ENSP00000509078.1:n.*137G=
ENST00000690595.1:c.910G=	ENSP00000508979.1:p.Val304=
ENST00000691348.1:c.*137G=	ENSP00000509369.1:n.*137G=
ENST00000691410.1:c.*1162G=	ENSP00000508479.1:n.*1162G=
ENST00000693287.1:c.901G=	ENSP00000510264.1:p.Val301=
ENST00000693681.1:c.898G=	ENSP00000510789.1:p.Val300=
ENST00000233838.9:c.1585G= MANE Select	ENSP00000233838.3:p.Val529=
ENST00000233838.8:c.1585G=	ENSP00000233838.3:p.Val529=
ENST00000430215.7:c.1414G=	ENSP00000408045.3:p.Val472=
ENST00000465637.5:n.179-3832G=
NM_000821.5:c.1585G=	NP_000812.2:p.Val529=
NM_000821.6:c.1585G=	NP_000812.2:p.Val529=
NM_001142269.2:c.1414G=	NP_001135741.1:p.Val472=
NM_001142269.3:c.1414G=	NP_001135741.1:p.Val472=
XM_005264259.3:c.1585G=	XP_005264316.1:p.Val529=
XM_011532764.1:c.763G=	XP_011531066.1:p.Val255=
XM_011532765.1:c.763G=	XP_011531067.1:p.Val255=
XR_939677.1:n.1498G=
XM_005264259.5:c.1585G=	XP_005264316.1:p.Val529=
XM_011532764.3:c.763G=	XP_011531066.1:p.Val255=
XM_011532765.3:c.763G=	XP_011531067.1:p.Val255=
XM_017003803.2:c.1414G=	XP_016859292.1:p.Val472=
XR_001738703.2:n.1498G=
NM_000821.7:c.1585G= MANE Select	NP_000812.2:p.Val529=
NM_001142269.4:c.1414G=	NP_001135741.1:p.Val472=