Canonical Allele Identifier: CA1266825506

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553251T= , CM000664.2:g.85553251T=	GRCh38
NC_000002.11:g.85780374T= , CM000664.1:g.85780374T=	GRCh37
NC_000002.10:g.85633885T=	NCBI36
NG_011811.2:g.13284A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5180A=
ENST00000482662.2:n.3587A=
ENST00000685865.1:n.1539A=
ENST00000687250.1:n.1239A=
ENST00000687995.1:n.1488A=
ENST00000688205.1:c.*729A=	ENSP00000509673.1:n.*729A=
ENST00000688788.1:n.1375A=
ENST00000689276.1:c.1067A=	ENSP00000510012.1:p.Tyr356=
ENST00000689576.1:c.1136A=	ENSP00000508712.1:p.Tyr379=
ENST00000690108.1:c.*792A=	ENSP00000510617.1:n.*792A=
ENST00000690468.1:c.857A=	ENSP00000509078.1:p.Tyr286=
ENST00000690595.1:c.461A=	ENSP00000508979.1:p.Tyr154=
ENST00000691348.1:c.965A=	ENSP00000509369.1:p.Tyr322=
ENST00000691410.1:c.*713A=	ENSP00000508479.1:n.*713A=
ENST00000693287.1:c.452A=	ENSP00000510264.1:p.Tyr151=
ENST00000693681.1:c.449A=	ENSP00000510789.1:p.Tyr150=
ENST00000233838.9:c.1136A= MANE Select	ENSP00000233838.3:p.Tyr379=
ENST00000233838.8:c.1136A=	ENSP00000233838.3:p.Tyr379=
ENST00000430215.7:c.965A=	ENSP00000408045.3:p.Tyr322=
ENST00000465637.5:n.179-5247A=
ENST00000473665.1:n.629A=
ENST00000482662.1:n.553A=
NM_000821.5:c.1136A=	NP_000812.2:p.Tyr379=
NM_000821.6:c.1136A=	NP_000812.2:p.Tyr379=
NM_001142269.2:c.965A=	NP_001135741.1:p.Tyr322=
NM_001142269.3:c.965A=	NP_001135741.1:p.Tyr322=
XM_005264259.3:c.1136A=	XP_005264316.1:p.Tyr379=
XM_011532764.1:c.314A=	XP_011531066.1:p.Tyr105=
XM_011532765.1:c.314A=	XP_011531067.1:p.Tyr105=
XR_939677.1:n.1201A=
XM_005264259.5:c.1136A=	XP_005264316.1:p.Tyr379=
XM_011532764.3:c.314A=	XP_011531066.1:p.Tyr105=
XM_011532765.3:c.314A=	XP_011531067.1:p.Tyr105=
XM_017003803.2:c.965A=	XP_016859292.1:p.Tyr322=
XR_001738703.2:n.1201A=
NM_000821.7:c.1136A= MANE Select	NP_000812.2:p.Tyr379=
NM_001142269.4:c.965A=	NP_001135741.1:p.Tyr322=