Canonical Allele Identifier: CA1266824935

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551941A= , CM000664.2:g.85551941A=	GRCh38
NC_000002.11:g.85779064A= , CM000664.1:g.85779064A=	GRCh37
NC_000002.10:g.85632575A=	NCBI36
NG_011811.2:g.14594T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5958T=
ENST00000482662.2:n.4365T=
ENST00000685865.1:n.2317T=
ENST00000687250.1:n.2017T=
ENST00000687995.1:n.1832T=
ENST00000688205.1:c.*1073T=	ENSP00000509673.1:n.*1073T=
ENST00000688788.1:n.1719T=
ENST00000689276.1:c.1411T=	ENSP00000510012.1:p.Ser471=
ENST00000689576.1:c.*99T=	ENSP00000508712.1:n.*99T=
ENST00000690108.1:c.*1136T=	ENSP00000510617.1:n.*1136T=
ENST00000690468.1:c.*32T=	ENSP00000509078.1:n.*32T=
ENST00000690595.1:c.805T=	ENSP00000508979.1:p.Ser269=
ENST00000691348.1:c.*32T=	ENSP00000509369.1:n.*32T=
ENST00000691410.1:c.*1057T=	ENSP00000508479.1:n.*1057T=
ENST00000693287.1:c.796T=	ENSP00000510264.1:p.Ser266=
ENST00000693681.1:c.793T=	ENSP00000510789.1:p.Ser265=
ENST00000233838.9:c.1480T= MANE Select	ENSP00000233838.3:p.Ser494=
ENST00000233838.8:c.1480T=	ENSP00000233838.3:p.Ser494=
ENST00000430215.7:c.1309T=	ENSP00000408045.3:p.Ser437=
ENST00000465637.5:n.179-3937T=
NM_000821.5:c.1480T=	NP_000812.2:p.Ser494=
NM_000821.6:c.1480T=	NP_000812.2:p.Ser494=
NM_001142269.2:c.1309T=	NP_001135741.1:p.Ser437=
NM_001142269.3:c.1309T=	NP_001135741.1:p.Ser437=
XM_005264259.3:c.1480T=	XP_005264316.1:p.Ser494=
XM_011532764.1:c.658T=	XP_011531066.1:p.Ser220=
XM_011532765.1:c.658T=	XP_011531067.1:p.Ser220=
XR_939677.1:n.1393T=
XM_005264259.5:c.1480T=	XP_005264316.1:p.Ser494=
XM_011532764.3:c.658T=	XP_011531066.1:p.Ser220=
XM_011532765.3:c.658T=	XP_011531067.1:p.Ser220=
XM_017003803.2:c.1309T=	XP_016859292.1:p.Ser437=
XR_001738703.2:n.1393T=
NM_000821.7:c.1480T= MANE Select	NP_000812.2:p.Ser494=
NM_001142269.4:c.1309T=	NP_001135741.1:p.Ser437=