Canonical Allele Identifier: CA1266825361

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85552959G= , CM000664.2:g.85552959G=	GRCh38
NC_000002.11:g.85780082G= , CM000664.1:g.85780082G=	GRCh37
NC_000002.10:g.85633593G=	NCBI36
NG_011811.2:g.13576C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5311C=
ENST00000482662.2:n.3718C=
ENST00000685865.1:n.1670C=
ENST00000687250.1:n.1370C=
ENST00000687995.1:n.1619C=
ENST00000688205.1:c.*860C=	ENSP00000509673.1:n.*860C=
ENST00000688788.1:n.1506C=
ENST00000689276.1:c.1198C=	ENSP00000510012.1:p.Leu400=
ENST00000689576.1:c.1267C=	ENSP00000508712.1:p.Leu423=
ENST00000690108.1:c.*923C=	ENSP00000510617.1:n.*923C=
ENST00000690468.1:c.988C=	ENSP00000509078.1:p.Leu330=
ENST00000690595.1:c.592C=	ENSP00000508979.1:p.Leu198=
ENST00000691348.1:c.1096C=	ENSP00000509369.1:p.Leu366=
ENST00000691410.1:c.*844C=	ENSP00000508479.1:n.*844C=
ENST00000693287.1:c.583C=	ENSP00000510264.1:p.Leu195=
ENST00000693681.1:c.580C=	ENSP00000510789.1:p.Leu194=
ENST00000233838.9:c.1267C= MANE Select	ENSP00000233838.3:p.Leu423=
ENST00000233838.8:c.1267C=	ENSP00000233838.3:p.Leu423=
ENST00000430215.7:c.1096C=	ENSP00000408045.3:p.Leu366=
ENST00000465637.5:n.179-4955C=
ENST00000473665.1:n.760C=
ENST00000482662.1:n.684C=
NM_000821.5:c.1267C=	NP_000812.2:p.Leu423=
NM_000821.6:c.1267C=	NP_000812.2:p.Leu423=
NM_001142269.2:c.1096C=	NP_001135741.1:p.Leu366=
NM_001142269.3:c.1096C=	NP_001135741.1:p.Leu366=
XM_005264259.3:c.1267C=	XP_005264316.1:p.Leu423=
XM_011532764.1:c.445C=	XP_011531066.1:p.Leu149=
XM_011532765.1:c.445C=	XP_011531067.1:p.Leu149=
XR_939677.1:n.1332C=
XM_005264259.5:c.1267C=	XP_005264316.1:p.Leu423=
XM_011532764.3:c.445C=	XP_011531066.1:p.Leu149=
XM_011532765.3:c.445C=	XP_011531067.1:p.Leu149=
XM_017003803.2:c.1096C=	XP_016859292.1:p.Leu366=
XR_001738703.2:n.1332C=
NM_000821.7:c.1267C= MANE Select	NP_000812.2:p.Leu423=
NM_001142269.4:c.1096C=	NP_001135741.1:p.Leu366=