Canonical Allele Identifier: CA1266827786

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85558966G= , CM000664.2:g.85558966G=	GRCh38
NC_000002.11:g.85786089G= , CM000664.1:g.85786089G=	GRCh37
NC_000002.10:g.85639600G=	NCBI36
NG_011811.2:g.7569C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.110C=
ENST00000482662.2:n.391C=
ENST00000496962.2:c.324C=	ENSP00000508856.1:p.Arg108=
ENST00000685865.1:n.416C=
ENST00000687250.1:n.427C=
ENST00000687995.1:n.365C=
ENST00000688205.1:c.324C=	ENSP00000509673.1:p.Arg108=
ENST00000688788.1:n.416C=
ENST00000689276.1:c.324C=	ENSP00000510012.1:p.Arg108=
ENST00000689576.1:c.324C=	ENSP00000508712.1:p.Arg108=
ENST00000690108.1:c.324C=	ENSP00000510617.1:p.Arg108=
ENST00000690468.1:c.153C=	ENSP00000509078.1:p.Arg51=
ENST00000690595.1:c.214+1849C=	ENSP00000508979.1:n.214+1849C=
ENST00000691348.1:c.153C=	ENSP00000509369.1:p.Arg51=
ENST00000691410.1:c.324C=	ENSP00000508479.1:p.Arg108=
ENST00000693287.1:c.-67+2420C=	ENSP00000510264.1:n.-67+2420C=
ENST00000693681.1:c.153C=	ENSP00000510789.1:p.Arg51=
ENST00000233838.9:c.324C= MANE Select	ENSP00000233838.3:p.Arg108=
ENST00000233838.8:c.324C=	ENSP00000233838.3:p.Arg108=
ENST00000421496.5:c.153C=	ENSP00000400384.1:p.Arg51=
ENST00000423570.5:c.324C=	ENSP00000389426.1:p.Arg108=
ENST00000428479.3:c.153C=	ENSP00000390748.3:p.Arg51=
ENST00000430215.7:c.153C=	ENSP00000408045.3:p.Arg51=
ENST00000465637.5:n.178+40C=
ENST00000481541.1:n.218C=
ENST00000496962.1:n.443C=
NM_000821.5:c.324C=	NP_000812.2:p.Arg108=
NM_000821.6:c.324C=	NP_000812.2:p.Arg108=
NM_001142269.2:c.153C=	NP_001135741.1:p.Arg51=
NM_001142269.3:c.153C=	NP_001135741.1:p.Arg51=
NM_001311312.1:c.324C=	NP_001298241.1:p.Arg108=
XM_005264259.3:c.324C=	XP_005264316.1:p.Arg108=
XM_011532764.1:c.-335C=	XP_011531066.1:n.-335C=
XM_011532765.1:c.-335C=	XP_011531067.1:n.-335C=
XR_939677.1:n.389C=
XM_005264259.5:c.324C=	XP_005264316.1:p.Arg108=
XM_011532764.3:c.-335C=	XP_011531066.1:n.-335C=
XM_011532765.3:c.-335C=	XP_011531067.1:n.-335C=
XM_017003803.2:c.153C=	XP_016859292.1:p.Arg51=
XR_001738703.2:n.389C=
NM_000821.7:c.324C= MANE Select	NP_000812.2:p.Arg108=
NM_001142269.4:c.153C=	NP_001135741.1:p.Arg51=
NM_001311312.2:c.324C=	NP_001298241.1:p.Arg108=