Canonical Allele Identifier: CA1266827783

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85558953C= , CM000664.2:g.85558953C=	GRCh38
NC_000002.11:g.85786076C= , CM000664.1:g.85786076C=	GRCh37
NC_000002.10:g.85639587C=	NCBI36
NG_011811.2:g.7582G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.123G=
ENST00000482662.2:n.404G=
ENST00000496962.2:c.337G=	ENSP00000508856.1:p.Asp113=
ENST00000685865.1:n.429G=
ENST00000687250.1:n.440G=
ENST00000687995.1:n.378G=
ENST00000688205.1:c.337G=	ENSP00000509673.1:p.Asp113=
ENST00000688788.1:n.429G=
ENST00000689276.1:c.337G=	ENSP00000510012.1:p.Asp113=
ENST00000689576.1:c.337G=	ENSP00000508712.1:p.Asp113=
ENST00000690108.1:c.337G=	ENSP00000510617.1:p.Asp113=
ENST00000690468.1:c.166G=	ENSP00000509078.1:p.Asp56=
ENST00000690595.1:c.214+1862G=	ENSP00000508979.1:n.214+1862G=
ENST00000691348.1:c.166G=	ENSP00000509369.1:p.Asp56=
ENST00000691410.1:c.337G=	ENSP00000508479.1:p.Asp113=
ENST00000693287.1:c.-67+2433G=	ENSP00000510264.1:n.-67+2433G=
ENST00000693681.1:c.166G=	ENSP00000510789.1:p.Asp56=
ENST00000233838.9:c.337G= MANE Select	ENSP00000233838.3:p.Asp113=
ENST00000233838.8:c.337G=	ENSP00000233838.3:p.Asp113=
ENST00000421496.5:c.166G=	ENSP00000400384.1:p.Asp56=
ENST00000423570.5:c.337G=	ENSP00000389426.1:p.Asp113=
ENST00000428479.3:c.166G=	ENSP00000390748.3:p.Asp56=
ENST00000430215.7:c.166G=	ENSP00000408045.3:p.Asp56=
ENST00000465637.5:n.178+53G=
ENST00000481541.1:n.231G=
ENST00000496962.1:n.456G=
NM_000821.5:c.337G=	NP_000812.2:p.Asp113=
NM_000821.6:c.337G=	NP_000812.2:p.Asp113=
NM_001142269.2:c.166G=	NP_001135741.1:p.Asp56=
NM_001142269.3:c.166G=	NP_001135741.1:p.Asp56=
NM_001311312.1:c.337G=	NP_001298241.1:p.Asp113=
XM_005264259.3:c.337G=	XP_005264316.1:p.Asp113=
XM_011532764.1:c.-322G=	XP_011531066.1:n.-322G=
XM_011532765.1:c.-322G=	XP_011531067.1:n.-322G=
XR_939677.1:n.402G=
XM_005264259.5:c.337G=	XP_005264316.1:p.Asp113=
XM_011532764.3:c.-322G=	XP_011531066.1:n.-322G=
XM_011532765.3:c.-322G=	XP_011531067.1:n.-322G=
XM_017003803.2:c.166G=	XP_016859292.1:p.Asp56=
XR_001738703.2:n.402G=
NM_000821.7:c.337G= MANE Select	NP_000812.2:p.Asp113=
NM_001142269.4:c.166G=	NP_001135741.1:p.Asp56=
NM_001311312.2:c.337G=	NP_001298241.1:p.Asp113=