Canonical Allele Identifier: CA1266825379

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85552990C= , CM000664.2:g.85552990C=	GRCh38
NC_000002.11:g.85780113C= , CM000664.1:g.85780113C=	GRCh37
NC_000002.10:g.85633624C=	NCBI36
NG_011811.2:g.13545G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5280G=
ENST00000482662.2:n.3687G=
ENST00000685865.1:n.1639G=
ENST00000687250.1:n.1339G=
ENST00000687995.1:n.1588G=
ENST00000688205.1:c.*829G=	ENSP00000509673.1:n.*829G=
ENST00000688788.1:n.1475G=
ENST00000689276.1:c.1167G=	ENSP00000510012.1:p.Lys389=
ENST00000689576.1:c.1236G=	ENSP00000508712.1:p.Lys412=
ENST00000690108.1:c.*892G=	ENSP00000510617.1:n.*892G=
ENST00000690468.1:c.957G=	ENSP00000509078.1:p.Lys319=
ENST00000690595.1:c.561G=	ENSP00000508979.1:p.Lys187=
ENST00000691348.1:c.1065G=	ENSP00000509369.1:p.Lys355=
ENST00000691410.1:c.*813G=	ENSP00000508479.1:n.*813G=
ENST00000693287.1:c.552G=	ENSP00000510264.1:p.Lys184=
ENST00000693681.1:c.549G=	ENSP00000510789.1:p.Lys183=
ENST00000233838.9:c.1236G= MANE Select	ENSP00000233838.3:p.Lys412=
ENST00000233838.8:c.1236G=	ENSP00000233838.3:p.Lys412=
ENST00000430215.7:c.1065G=	ENSP00000408045.3:p.Lys355=
ENST00000465637.5:n.179-4986G=
ENST00000473665.1:n.729G=
ENST00000482662.1:n.653G=
NM_000821.5:c.1236G=	NP_000812.2:p.Lys412=
NM_000821.6:c.1236G=	NP_000812.2:p.Lys412=
NM_001142269.2:c.1065G=	NP_001135741.1:p.Lys355=
NM_001142269.3:c.1065G=	NP_001135741.1:p.Lys355=
XM_005264259.3:c.1236G=	XP_005264316.1:p.Lys412=
XM_011532764.1:c.414G=	XP_011531066.1:p.Lys138=
XM_011532765.1:c.414G=	XP_011531067.1:p.Lys138=
XR_939677.1:n.1301G=
XM_005264259.5:c.1236G=	XP_005264316.1:p.Lys412=
XM_011532764.3:c.414G=	XP_011531066.1:p.Lys138=
XM_011532765.3:c.414G=	XP_011531067.1:p.Lys138=
XM_017003803.2:c.1065G=	XP_016859292.1:p.Lys355=
XR_001738703.2:n.1301G=
NM_000821.7:c.1236G= MANE Select	NP_000812.2:p.Lys412=
NM_001142269.4:c.1065G=	NP_001135741.1:p.Lys355=