Canonical Allele Identifier: CA1266824887

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551826A= , CM000664.2:g.85551826A=	GRCh38
NC_000002.11:g.85778949A= , CM000664.1:g.85778949A=	GRCh37
NC_000002.10:g.85632460A=	NCBI36
NG_011811.2:g.14709T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.6073T=
ENST00000482662.2:n.4480T=
ENST00000685865.1:n.2432T=
ENST00000687250.1:n.2132T=
ENST00000687995.1:n.1947T=
ENST00000688205.1:c.*1188T=	ENSP00000509673.1:n.*1188T=
ENST00000688788.1:n.1834T=
ENST00000689276.1:c.1526T=	ENSP00000510012.1:p.Ile509=
ENST00000689576.1:c.*214T=	ENSP00000508712.1:n.*214T=
ENST00000690108.1:c.*1251T=	ENSP00000510617.1:n.*1251T=
ENST00000690468.1:c.*147T=	ENSP00000509078.1:n.*147T=
ENST00000690595.1:c.920T=	ENSP00000508979.1:p.Ile307=
ENST00000691348.1:c.*147T=	ENSP00000509369.1:n.*147T=
ENST00000691410.1:c.*1172T=	ENSP00000508479.1:n.*1172T=
ENST00000693287.1:c.911T=	ENSP00000510264.1:p.Ile304=
ENST00000693681.1:c.908T=	ENSP00000510789.1:p.Ile303=
ENST00000233838.9:c.1595T= MANE Select	ENSP00000233838.3:p.Ile532=
ENST00000233838.8:c.1595T=	ENSP00000233838.3:p.Ile532=
ENST00000430215.7:c.1424T=	ENSP00000408045.3:p.Ile475=
ENST00000465637.5:n.179-3822T=
NM_000821.5:c.1595T=	NP_000812.2:p.Ile532=
NM_000821.6:c.1595T=	NP_000812.2:p.Ile532=
NM_001142269.2:c.1424T=	NP_001135741.1:p.Ile475=
NM_001142269.3:c.1424T=	NP_001135741.1:p.Ile475=
XM_005264259.3:c.1595T=	XP_005264316.1:p.Ile532=
XM_011532764.1:c.773T=	XP_011531066.1:p.Ile258=
XM_011532765.1:c.773T=	XP_011531067.1:p.Ile258=
XR_939677.1:n.1508T=
XM_005264259.5:c.1595T=	XP_005264316.1:p.Ile532=
XM_011532764.3:c.773T=	XP_011531066.1:p.Ile258=
XM_011532765.3:c.773T=	XP_011531067.1:p.Ile258=
XM_017003803.2:c.1424T=	XP_016859292.1:p.Ile475=
XR_001738703.2:n.1508T=
NM_000821.7:c.1595T= MANE Select	NP_000812.2:p.Ile532=
NM_001142269.4:c.1424T=	NP_001135741.1:p.Ile475=