Canonical Allele Identifier: CA1266824950

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551971G= , CM000664.2:g.85551971G=	GRCh38
NC_000002.11:g.85779094G= , CM000664.1:g.85779094G=	GRCh37
NC_000002.10:g.85632605G=	NCBI36
NG_011811.2:g.14564C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5928C=
ENST00000482662.2:n.4335C=
ENST00000685865.1:n.2287C=
ENST00000687250.1:n.1987C=
ENST00000687995.1:n.1802C=
ENST00000688205.1:c.*1043C=	ENSP00000509673.1:n.*1043C=
ENST00000688788.1:n.1689C=
ENST00000689276.1:c.1381C=	ENSP00000510012.1:p.Pro461=
ENST00000689576.1:c.*69C=	ENSP00000508712.1:n.*69C=
ENST00000690108.1:c.*1106C=	ENSP00000510617.1:n.*1106C=
ENST00000690468.1:c.*2C=	ENSP00000509078.1:n.*2C=
ENST00000690595.1:c.775C=	ENSP00000508979.1:p.Pro259=
ENST00000691348.1:c.*2C=	ENSP00000509369.1:n.*2C=
ENST00000691410.1:c.*1027C=	ENSP00000508479.1:n.*1027C=
ENST00000693287.1:c.766C=	ENSP00000510264.1:p.Pro256=
ENST00000693681.1:c.763C=	ENSP00000510789.1:p.Pro255=
ENST00000233838.9:c.1450C= MANE Select	ENSP00000233838.3:p.Pro484=
ENST00000233838.8:c.1450C=	ENSP00000233838.3:p.Pro484=
ENST00000430215.7:c.1279C=	ENSP00000408045.3:p.Pro427=
ENST00000465637.5:n.179-3967C=
NM_000821.5:c.1450C=	NP_000812.2:p.Pro484=
NM_000821.6:c.1450C=	NP_000812.2:p.Pro484=
NM_001142269.2:c.1279C=	NP_001135741.1:p.Pro427=
NM_001142269.3:c.1279C=	NP_001135741.1:p.Pro427=
XM_005264259.3:c.1450C=	XP_005264316.1:p.Pro484=
XM_011532764.1:c.628C=	XP_011531066.1:p.Pro210=
XM_011532765.1:c.628C=	XP_011531067.1:p.Pro210=
XR_939677.1:n.1363C=
XM_005264259.5:c.1450C=	XP_005264316.1:p.Pro484=
XM_011532764.3:c.628C=	XP_011531066.1:p.Pro210=
XM_011532765.3:c.628C=	XP_011531067.1:p.Pro210=
XM_017003803.2:c.1279C=	XP_016859292.1:p.Pro427=
XR_001738703.2:n.1363C=
NM_000821.7:c.1450C= MANE Select	NP_000812.2:p.Pro484=
NM_001142269.4:c.1279C=	NP_001135741.1:p.Pro427=