Canonical Allele Identifier: CA1266824897

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551841G= , CM000664.2:g.85551841G=	GRCh38
NC_000002.11:g.85778964G= , CM000664.1:g.85778964G=	GRCh37
NC_000002.10:g.85632475G=	NCBI36
NG_011811.2:g.14694C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6058C=
ENST00000482662.2:n.4465C=
ENST00000685865.1:n.2417C=
ENST00000687250.1:n.2117C=
ENST00000687995.1:n.1932C=
ENST00000688205.1:c.*1173C=	ENSP00000509673.1:n.*1173C=
ENST00000688788.1:n.1819C=
ENST00000689276.1:c.1511C=	ENSP00000510012.1:p.Thr504=
ENST00000689576.1:c.*199C=	ENSP00000508712.1:n.*199C=
ENST00000690108.1:c.*1236C=	ENSP00000510617.1:n.*1236C=
ENST00000690468.1:c.*132C=	ENSP00000509078.1:n.*132C=
ENST00000690595.1:c.905C=	ENSP00000508979.1:p.Thr302=
ENST00000691348.1:c.*132C=	ENSP00000509369.1:n.*132C=
ENST00000691410.1:c.*1157C=	ENSP00000508479.1:n.*1157C=
ENST00000693287.1:c.896C=	ENSP00000510264.1:p.Thr299=
ENST00000693681.1:c.893C=	ENSP00000510789.1:p.Thr298=
ENST00000233838.9:c.1580C= MANE Select	ENSP00000233838.3:p.Thr527=
ENST00000233838.8:c.1580C=	ENSP00000233838.3:p.Thr527=
ENST00000430215.7:c.1409C=	ENSP00000408045.3:p.Thr470=
ENST00000465637.5:n.179-3837C=
NM_000821.5:c.1580C=	NP_000812.2:p.Thr527=
NM_000821.6:c.1580C=	NP_000812.2:p.Thr527=
NM_001142269.2:c.1409C=	NP_001135741.1:p.Thr470=
NM_001142269.3:c.1409C=	NP_001135741.1:p.Thr470=
XM_005264259.3:c.1580C=	XP_005264316.1:p.Thr527=
XM_011532764.1:c.758C=	XP_011531066.1:p.Thr253=
XM_011532765.1:c.758C=	XP_011531067.1:p.Thr253=
XR_939677.1:n.1493C=
XM_005264259.5:c.1580C=	XP_005264316.1:p.Thr527=
XM_011532764.3:c.758C=	XP_011531066.1:p.Thr253=
XM_011532765.3:c.758C=	XP_011531067.1:p.Thr253=
XM_017003803.2:c.1409C=	XP_016859292.1:p.Thr470=
XR_001738703.2:n.1493C=
NM_000821.7:c.1580C= MANE Select	NP_000812.2:p.Thr527=
NM_001142269.4:c.1409C=	NP_001135741.1:p.Thr470=