Canonical Allele Identifier: CA1266825508

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553256C= , CM000664.2:g.85553256C=	GRCh38
NC_000002.11:g.85780379C= , CM000664.1:g.85780379C=	GRCh37
NC_000002.10:g.85633890C=	NCBI36
NG_011811.2:g.13279G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5175G=
ENST00000482662.2:n.3582G=
ENST00000685865.1:n.1534G=
ENST00000687250.1:n.1234G=
ENST00000687995.1:n.1483G=
ENST00000688205.1:c.*724G=	ENSP00000509673.1:n.*724G=
ENST00000688788.1:n.1370G=
ENST00000689276.1:c.1062G=	ENSP00000510012.1:p.Leu354=
ENST00000689576.1:c.1131G=	ENSP00000508712.1:p.Leu377=
ENST00000690108.1:c.*787G=	ENSP00000510617.1:n.*787G=
ENST00000690468.1:c.852G=	ENSP00000509078.1:p.Leu284=
ENST00000690595.1:c.456G=	ENSP00000508979.1:p.Leu152=
ENST00000691348.1:c.960G=	ENSP00000509369.1:p.Leu320=
ENST00000691410.1:c.*708G=	ENSP00000508479.1:n.*708G=
ENST00000693287.1:c.447G=	ENSP00000510264.1:p.Leu149=
ENST00000693681.1:c.444G=	ENSP00000510789.1:p.Leu148=
ENST00000233838.9:c.1131G= MANE Select	ENSP00000233838.3:p.Leu377=
ENST00000233838.8:c.1131G=	ENSP00000233838.3:p.Leu377=
ENST00000430215.7:c.960G=	ENSP00000408045.3:p.Leu320=
ENST00000465637.5:n.179-5252G=
ENST00000473665.1:n.624G=
ENST00000482662.1:n.548G=
NM_000821.5:c.1131G=	NP_000812.2:p.Leu377=
NM_000821.6:c.1131G=	NP_000812.2:p.Leu377=
NM_001142269.2:c.960G=	NP_001135741.1:p.Leu320=
NM_001142269.3:c.960G=	NP_001135741.1:p.Leu320=
XM_005264259.3:c.1131G=	XP_005264316.1:p.Leu377=
XM_011532764.1:c.309G=	XP_011531066.1:p.Leu103=
XM_011532765.1:c.309G=	XP_011531067.1:p.Leu103=
XR_939677.1:n.1196G=
XM_005264259.5:c.1131G=	XP_005264316.1:p.Leu377=
XM_011532764.3:c.309G=	XP_011531066.1:p.Leu103=
XM_011532765.3:c.309G=	XP_011531067.1:p.Leu103=
XM_017003803.2:c.960G=	XP_016859292.1:p.Leu320=
XR_001738703.2:n.1196G=
NM_000821.7:c.1131G= MANE Select	NP_000812.2:p.Leu377=
NM_001142269.4:c.960G=	NP_001135741.1:p.Leu320=