Canonical Allele Identifier: CA1266824940

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551947C= , CM000664.2:g.85551947C=	GRCh38
NC_000002.11:g.85779070C= , CM000664.1:g.85779070C=	GRCh37
NC_000002.10:g.85632581C=	NCBI36
NG_011811.2:g.14588G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000473665.2:n.5952G=
ENST00000482662.2:n.4359G=
ENST00000685865.1:n.2311G=
ENST00000687250.1:n.2011G=
ENST00000687995.1:n.1826G=
ENST00000688205.1:c.*1067G=	ENSP00000509673.1:n.*1067G=
ENST00000688788.1:n.1713G=
ENST00000689276.1:c.1405G=	ENSP00000510012.1:p.Ala469=
ENST00000689576.1:c.*93G=	ENSP00000508712.1:n.*93G=
ENST00000690108.1:c.*1130G=	ENSP00000510617.1:n.*1130G=
ENST00000690468.1:c.*26G=	ENSP00000509078.1:n.*26G=
ENST00000690595.1:c.799G=	ENSP00000508979.1:p.Ala267=
ENST00000691348.1:c.*26G=	ENSP00000509369.1:n.*26G=
ENST00000691410.1:c.*1051G=	ENSP00000508479.1:n.*1051G=
ENST00000693287.1:c.790G=	ENSP00000510264.1:p.Ala264=
ENST00000693681.1:c.787G=	ENSP00000510789.1:p.Ala263=
ENST00000233838.9:c.1474G= MANE Select	ENSP00000233838.3:p.Ala492=
ENST00000233838.8:c.1474G=	ENSP00000233838.3:p.Ala492=
ENST00000430215.7:c.1303G=	ENSP00000408045.3:p.Ala435=
ENST00000465637.5:n.179-3943G=
NM_000821.5:c.1474G=	NP_000812.2:p.Ala492=
NM_000821.6:c.1474G=	NP_000812.2:p.Ala492=
NM_001142269.2:c.1303G=	NP_001135741.1:p.Ala435=
NM_001142269.3:c.1303G=	NP_001135741.1:p.Ala435=
XM_005264259.3:c.1474G=	XP_005264316.1:p.Ala492=
XM_011532764.1:c.652G=	XP_011531066.1:p.Ala218=
XM_011532765.1:c.652G=	XP_011531067.1:p.Ala218=
XR_939677.1:n.1387G=
XM_005264259.5:c.1474G=	XP_005264316.1:p.Ala492=
XM_011532764.3:c.652G=	XP_011531066.1:p.Ala218=
XM_011532765.3:c.652G=	XP_011531067.1:p.Ala218=
XM_017003803.2:c.1303G=	XP_016859292.1:p.Ala435=
XR_001738703.2:n.1387G=
NM_000821.7:c.1474G= MANE Select	NP_000812.2:p.Ala492=
NM_001142269.4:c.1303G=	NP_001135741.1:p.Ala435=