Canonical Allele Identifier: CA1266824949

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551970G= , CM000664.2:g.85551970G=	GRCh38
NC_000002.11:g.85779093G= , CM000664.1:g.85779093G=	GRCh37
NC_000002.10:g.85632604G=	NCBI36
NG_011811.2:g.14565C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5929C=
ENST00000482662.2:n.4336C=
ENST00000685865.1:n.2288C=
ENST00000687250.1:n.1988C=
ENST00000687995.1:n.1803C=
ENST00000688205.1:c.*1044C=	ENSP00000509673.1:n.*1044C=
ENST00000688788.1:n.1690C=
ENST00000689276.1:c.1382C=	ENSP00000510012.1:p.Pro461=
ENST00000689576.1:c.*70C=	ENSP00000508712.1:n.*70C=
ENST00000690108.1:c.*1107C=	ENSP00000510617.1:n.*1107C=
ENST00000690468.1:c.*3C=	ENSP00000509078.1:n.*3C=
ENST00000690595.1:c.776C=	ENSP00000508979.1:p.Pro259=
ENST00000691348.1:c.*3C=	ENSP00000509369.1:n.*3C=
ENST00000691410.1:c.*1028C=	ENSP00000508479.1:n.*1028C=
ENST00000693287.1:c.767C=	ENSP00000510264.1:p.Pro256=
ENST00000693681.1:c.764C=	ENSP00000510789.1:p.Pro255=
ENST00000233838.9:c.1451C= MANE Select	ENSP00000233838.3:p.Pro484=
ENST00000233838.8:c.1451C=	ENSP00000233838.3:p.Pro484=
ENST00000430215.7:c.1280C=	ENSP00000408045.3:p.Pro427=
ENST00000465637.5:n.179-3966C=
NM_000821.5:c.1451C=	NP_000812.2:p.Pro484=
NM_000821.6:c.1451C=	NP_000812.2:p.Pro484=
NM_001142269.2:c.1280C=	NP_001135741.1:p.Pro427=
NM_001142269.3:c.1280C=	NP_001135741.1:p.Pro427=
XM_005264259.3:c.1451C=	XP_005264316.1:p.Pro484=
XM_011532764.1:c.629C=	XP_011531066.1:p.Pro210=
XM_011532765.1:c.629C=	XP_011531067.1:p.Pro210=
XR_939677.1:n.1364C=
XM_005264259.5:c.1451C=	XP_005264316.1:p.Pro484=
XM_011532764.3:c.629C=	XP_011531066.1:p.Pro210=
XM_011532765.3:c.629C=	XP_011531067.1:p.Pro210=
XM_017003803.2:c.1280C=	XP_016859292.1:p.Pro427=
XR_001738703.2:n.1364C=
NM_000821.7:c.1451C= MANE Select	NP_000812.2:p.Pro484=
NM_001142269.4:c.1280C=	NP_001135741.1:p.Pro427=