Canonical Allele Identifier: CA1266824924

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551922G= , CM000664.2:g.85551922G=	GRCh38
NC_000002.11:g.85779045G= , CM000664.1:g.85779045G=	GRCh37
NC_000002.10:g.85632556G=	NCBI36
NG_011811.2:g.14613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5977C=
ENST00000482662.2:n.4384C=
ENST00000685865.1:n.2336C=
ENST00000687250.1:n.2036C=
ENST00000687995.1:n.1851C=
ENST00000688205.1:c.*1092C=	ENSP00000509673.1:n.*1092C=
ENST00000688788.1:n.1738C=
ENST00000689276.1:c.1430C=	ENSP00000510012.1:p.Ser477=
ENST00000689576.1:c.*118C=	ENSP00000508712.1:n.*118C=
ENST00000690108.1:c.*1155C=	ENSP00000510617.1:n.*1155C=
ENST00000690468.1:c.*51C=	ENSP00000509078.1:n.*51C=
ENST00000690595.1:c.824C=	ENSP00000508979.1:p.Ser275=
ENST00000691348.1:c.*51C=	ENSP00000509369.1:n.*51C=
ENST00000691410.1:c.*1076C=	ENSP00000508479.1:n.*1076C=
ENST00000693287.1:c.815C=	ENSP00000510264.1:p.Ser272=
ENST00000693681.1:c.812C=	ENSP00000510789.1:p.Ser271=
ENST00000233838.9:c.1499C= MANE Select	ENSP00000233838.3:p.Ser500=
ENST00000233838.8:c.1499C=	ENSP00000233838.3:p.Ser500=
ENST00000430215.7:c.1328C=	ENSP00000408045.3:p.Ser443=
ENST00000465637.5:n.179-3918C=
NM_000821.5:c.1499C=	NP_000812.2:p.Ser500=
NM_000821.6:c.1499C=	NP_000812.2:p.Ser500=
NM_001142269.2:c.1328C=	NP_001135741.1:p.Ser443=
NM_001142269.3:c.1328C=	NP_001135741.1:p.Ser443=
XM_005264259.3:c.1499C=	XP_005264316.1:p.Ser500=
XM_011532764.1:c.677C=	XP_011531066.1:p.Ser226=
XM_011532765.1:c.677C=	XP_011531067.1:p.Ser226=
XR_939677.1:n.1412C=
XM_005264259.5:c.1499C=	XP_005264316.1:p.Ser500=
XM_011532764.3:c.677C=	XP_011531066.1:p.Ser226=
XM_011532765.3:c.677C=	XP_011531067.1:p.Ser226=
XM_017003803.2:c.1328C=	XP_016859292.1:p.Ser443=
XR_001738703.2:n.1412C=
NM_000821.7:c.1499C= MANE Select	NP_000812.2:p.Ser500=
NM_001142269.4:c.1328C=	NP_001135741.1:p.Ser443=