Canonical Allele Identifier: CA1266824896

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551840A= , CM000664.2:g.85551840A=	GRCh38
NC_000002.11:g.85778963A= , CM000664.1:g.85778963A=	GRCh37
NC_000002.10:g.85632474A=	NCBI36
NG_011811.2:g.14695T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6059T=
ENST00000482662.2:n.4466T=
ENST00000685865.1:n.2418T=
ENST00000687250.1:n.2118T=
ENST00000687995.1:n.1933T=
ENST00000688205.1:c.*1174T=	ENSP00000509673.1:n.*1174T=
ENST00000688788.1:n.1820T=
ENST00000689276.1:c.1512T=	ENSP00000510012.1:p.Thr504=
ENST00000689576.1:c.*200T=	ENSP00000508712.1:n.*200T=
ENST00000690108.1:c.*1237T=	ENSP00000510617.1:n.*1237T=
ENST00000690468.1:c.*133T=	ENSP00000509078.1:n.*133T=
ENST00000690595.1:c.906T=	ENSP00000508979.1:p.Thr302=
ENST00000691348.1:c.*133T=	ENSP00000509369.1:n.*133T=
ENST00000691410.1:c.*1158T=	ENSP00000508479.1:n.*1158T=
ENST00000693287.1:c.897T=	ENSP00000510264.1:p.Thr299=
ENST00000693681.1:c.894T=	ENSP00000510789.1:p.Thr298=
ENST00000233838.9:c.1581T= MANE Select	ENSP00000233838.3:p.Thr527=
ENST00000233838.8:c.1581T=	ENSP00000233838.3:p.Thr527=
ENST00000430215.7:c.1410T=	ENSP00000408045.3:p.Thr470=
ENST00000465637.5:n.179-3836T=
NM_000821.5:c.1581T=	NP_000812.2:p.Thr527=
NM_000821.6:c.1581T=	NP_000812.2:p.Thr527=
NM_001142269.2:c.1410T=	NP_001135741.1:p.Thr470=
NM_001142269.3:c.1410T=	NP_001135741.1:p.Thr470=
XM_005264259.3:c.1581T=	XP_005264316.1:p.Thr527=
XM_011532764.1:c.759T=	XP_011531066.1:p.Thr253=
XM_011532765.1:c.759T=	XP_011531067.1:p.Thr253=
XR_939677.1:n.1494T=
XM_005264259.5:c.1581T=	XP_005264316.1:p.Thr527=
XM_011532764.3:c.759T=	XP_011531066.1:p.Thr253=
XM_011532765.3:c.759T=	XP_011531067.1:p.Thr253=
XM_017003803.2:c.1410T=	XP_016859292.1:p.Thr470=
XR_001738703.2:n.1494T=
NM_000821.7:c.1581T= MANE Select	NP_000812.2:p.Thr527=
NM_001142269.4:c.1410T=	NP_001135741.1:p.Thr470=