Canonical Allele Identifier: CA1266824899

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551846G= , CM000664.2:g.85551846G=	GRCh38
NC_000002.11:g.85778969G= , CM000664.1:g.85778969G=	GRCh37
NC_000002.10:g.85632480G=	NCBI36
NG_011811.2:g.14689C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6053C=
ENST00000482662.2:n.4460C=
ENST00000685865.1:n.2412C=
ENST00000687250.1:n.2112C=
ENST00000687995.1:n.1927C=
ENST00000688205.1:c.*1168C=	ENSP00000509673.1:n.*1168C=
ENST00000688788.1:n.1814C=
ENST00000689276.1:c.1506C=	ENSP00000510012.1:p.Asn502=
ENST00000689576.1:c.*194C=	ENSP00000508712.1:n.*194C=
ENST00000690108.1:c.*1231C=	ENSP00000510617.1:n.*1231C=
ENST00000690468.1:c.*127C=	ENSP00000509078.1:n.*127C=
ENST00000690595.1:c.900C=	ENSP00000508979.1:p.Asn300=
ENST00000691348.1:c.*127C=	ENSP00000509369.1:n.*127C=
ENST00000691410.1:c.*1152C=	ENSP00000508479.1:n.*1152C=
ENST00000693287.1:c.891C=	ENSP00000510264.1:p.Asn297=
ENST00000693681.1:c.888C=	ENSP00000510789.1:p.Asn296=
ENST00000233838.9:c.1575C= MANE Select	ENSP00000233838.3:p.Asn525=
ENST00000233838.8:c.1575C=	ENSP00000233838.3:p.Asn525=
ENST00000430215.7:c.1404C=	ENSP00000408045.3:p.Asn468=
ENST00000465637.5:n.179-3842C=
NM_000821.5:c.1575C=	NP_000812.2:p.Asn525=
NM_000821.6:c.1575C=	NP_000812.2:p.Asn525=
NM_001142269.2:c.1404C=	NP_001135741.1:p.Asn468=
NM_001142269.3:c.1404C=	NP_001135741.1:p.Asn468=
XM_005264259.3:c.1575C=	XP_005264316.1:p.Asn525=
XM_011532764.1:c.753C=	XP_011531066.1:p.Asn251=
XM_011532765.1:c.753C=	XP_011531067.1:p.Asn251=
XR_939677.1:n.1488C=
XM_005264259.5:c.1575C=	XP_005264316.1:p.Asn525=
XM_011532764.3:c.753C=	XP_011531066.1:p.Asn251=
XM_011532765.3:c.753C=	XP_011531067.1:p.Asn251=
XM_017003803.2:c.1404C=	XP_016859292.1:p.Asn468=
XR_001738703.2:n.1488C=
NM_000821.7:c.1575C= MANE Select	NP_000812.2:p.Asn525=
NM_001142269.4:c.1404C=	NP_001135741.1:p.Asn468=