Canonical Allele Identifier: CA1266824919

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551901A= , CM000664.2:g.85551901A=	GRCh38
NC_000002.11:g.85779024A= , CM000664.1:g.85779024A=	GRCh37
NC_000002.10:g.85632535A=	NCBI36
NG_011811.2:g.14634T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5998T=
ENST00000482662.2:n.4405T=
ENST00000685865.1:n.2357T=
ENST00000687250.1:n.2057T=
ENST00000687995.1:n.1872T=
ENST00000688205.1:c.*1113T=	ENSP00000509673.1:n.*1113T=
ENST00000688788.1:n.1759T=
ENST00000689276.1:c.1451T=	ENSP00000510012.1:p.Met484=
ENST00000689576.1:c.*139T=	ENSP00000508712.1:n.*139T=
ENST00000690108.1:c.*1176T=	ENSP00000510617.1:n.*1176T=
ENST00000690468.1:c.*72T=	ENSP00000509078.1:n.*72T=
ENST00000690595.1:c.845T=	ENSP00000508979.1:p.Met282=
ENST00000691348.1:c.*72T=	ENSP00000509369.1:n.*72T=
ENST00000691410.1:c.*1097T=	ENSP00000508479.1:n.*1097T=
ENST00000693287.1:c.836T=	ENSP00000510264.1:p.Met279=
ENST00000693681.1:c.833T=	ENSP00000510789.1:p.Met278=
ENST00000233838.9:c.1520T= MANE Select	ENSP00000233838.3:p.Met507=
ENST00000233838.8:c.1520T=	ENSP00000233838.3:p.Met507=
ENST00000430215.7:c.1349T=	ENSP00000408045.3:p.Met450=
ENST00000465637.5:n.179-3897T=
NM_000821.5:c.1520T=	NP_000812.2:p.Met507=
NM_000821.6:c.1520T=	NP_000812.2:p.Met507=
NM_001142269.2:c.1349T=	NP_001135741.1:p.Met450=
NM_001142269.3:c.1349T=	NP_001135741.1:p.Met450=
XM_005264259.3:c.1520T=	XP_005264316.1:p.Met507=
XM_011532764.1:c.698T=	XP_011531066.1:p.Met233=
XM_011532765.1:c.698T=	XP_011531067.1:p.Met233=
XR_939677.1:n.1433T=
XM_005264259.5:c.1520T=	XP_005264316.1:p.Met507=
XM_011532764.3:c.698T=	XP_011531066.1:p.Met233=
XM_011532765.3:c.698T=	XP_011531067.1:p.Met233=
XM_017003803.2:c.1349T=	XP_016859292.1:p.Met450=
XR_001738703.2:n.1433T=
NM_000821.7:c.1520T= MANE Select	NP_000812.2:p.Met507=
NM_001142269.4:c.1349T=	NP_001135741.1:p.Met450=