Canonical Allele Identifier: CA1266825402

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553024A= , CM000664.2:g.85553024A=	GRCh38
NC_000002.11:g.85780147A= , CM000664.1:g.85780147A=	GRCh37
NC_000002.10:g.85633658A=	NCBI36
NG_011811.2:g.13511T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5246T=
ENST00000482662.2:n.3653T=
ENST00000685865.1:n.1605T=
ENST00000687250.1:n.1305T=
ENST00000687995.1:n.1554T=
ENST00000688205.1:c.*795T=	ENSP00000509673.1:n.*795T=
ENST00000688788.1:n.1441T=
ENST00000689276.1:c.1133T=	ENSP00000510012.1:p.Met378=
ENST00000689576.1:c.1202T=	ENSP00000508712.1:p.Met401=
ENST00000690108.1:c.*858T=	ENSP00000510617.1:n.*858T=
ENST00000690468.1:c.923T=	ENSP00000509078.1:p.Met308=
ENST00000690595.1:c.527T=	ENSP00000508979.1:p.Met176=
ENST00000691348.1:c.1031T=	ENSP00000509369.1:p.Met344=
ENST00000691410.1:c.*779T=	ENSP00000508479.1:n.*779T=
ENST00000693287.1:c.518T=	ENSP00000510264.1:p.Met173=
ENST00000693681.1:c.515T=	ENSP00000510789.1:p.Met172=
ENST00000233838.9:c.1202T= MANE Select	ENSP00000233838.3:p.Met401=
ENST00000233838.8:c.1202T=	ENSP00000233838.3:p.Met401=
ENST00000430215.7:c.1031T=	ENSP00000408045.3:p.Met344=
ENST00000465637.5:n.179-5020T=
ENST00000473665.1:n.695T=
ENST00000482662.1:n.619T=
NM_000821.5:c.1202T=	NP_000812.2:p.Met401=
NM_000821.6:c.1202T=	NP_000812.2:p.Met401=
NM_001142269.2:c.1031T=	NP_001135741.1:p.Met344=
NM_001142269.3:c.1031T=	NP_001135741.1:p.Met344=
XM_005264259.3:c.1202T=	XP_005264316.1:p.Met401=
XM_011532764.1:c.380T=	XP_011531066.1:p.Met127=
XM_011532765.1:c.380T=	XP_011531067.1:p.Met127=
XR_939677.1:n.1267T=
XM_005264259.5:c.1202T=	XP_005264316.1:p.Met401=
XM_011532764.3:c.380T=	XP_011531066.1:p.Met127=
XM_011532765.3:c.380T=	XP_011531067.1:p.Met127=
XM_017003803.2:c.1031T=	XP_016859292.1:p.Met344=
XR_001738703.2:n.1267T=
NM_000821.7:c.1202T= MANE Select	NP_000812.2:p.Met401=
NM_001142269.4:c.1031T=	NP_001135741.1:p.Met344=