Canonical Allele Identifier: CA1266824943

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551952T= , CM000664.2:g.85551952T=	GRCh38
NC_000002.11:g.85779075T= , CM000664.1:g.85779075T=	GRCh37
NC_000002.10:g.85632586T=	NCBI36
NG_011811.2:g.14583A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5947A=
ENST00000482662.2:n.4354A=
ENST00000685865.1:n.2306A=
ENST00000687250.1:n.2006A=
ENST00000687995.1:n.1821A=
ENST00000688205.1:c.*1062A=	ENSP00000509673.1:n.*1062A=
ENST00000688788.1:n.1708A=
ENST00000689276.1:c.1400A=	ENSP00000510012.1:p.Gln467=
ENST00000689576.1:c.*88A=	ENSP00000508712.1:n.*88A=
ENST00000690108.1:c.*1125A=	ENSP00000510617.1:n.*1125A=
ENST00000690468.1:c.*21A=	ENSP00000509078.1:n.*21A=
ENST00000690595.1:c.794A=	ENSP00000508979.1:p.Gln265=
ENST00000691348.1:c.*21A=	ENSP00000509369.1:n.*21A=
ENST00000691410.1:c.*1046A=	ENSP00000508479.1:n.*1046A=
ENST00000693287.1:c.785A=	ENSP00000510264.1:p.Gln262=
ENST00000693681.1:c.782A=	ENSP00000510789.1:p.Gln261=
ENST00000233838.9:c.1469A= MANE Select	ENSP00000233838.3:p.Gln490=
ENST00000233838.8:c.1469A=	ENSP00000233838.3:p.Gln490=
ENST00000430215.7:c.1298A=	ENSP00000408045.3:p.Gln433=
ENST00000465637.5:n.179-3948A=
NM_000821.5:c.1469A=	NP_000812.2:p.Gln490=
NM_000821.6:c.1469A=	NP_000812.2:p.Gln490=
NM_001142269.2:c.1298A=	NP_001135741.1:p.Gln433=
NM_001142269.3:c.1298A=	NP_001135741.1:p.Gln433=
XM_005264259.3:c.1469A=	XP_005264316.1:p.Gln490=
XM_011532764.1:c.647A=	XP_011531066.1:p.Gln216=
XM_011532765.1:c.647A=	XP_011531067.1:p.Gln216=
XR_939677.1:n.1382A=
XM_005264259.5:c.1469A=	XP_005264316.1:p.Gln490=
XM_011532764.3:c.647A=	XP_011531066.1:p.Gln216=
XM_011532765.3:c.647A=	XP_011531067.1:p.Gln216=
XM_017003803.2:c.1298A=	XP_016859292.1:p.Gln433=
XR_001738703.2:n.1382A=
NM_000821.7:c.1469A= MANE Select	NP_000812.2:p.Gln490=
NM_001142269.4:c.1298A=	NP_001135741.1:p.Gln433=