Canonical Allele Identifier: CA1266824921

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551912T= , CM000664.2:g.85551912T=	GRCh38
NC_000002.11:g.85779035T= , CM000664.1:g.85779035T=	GRCh37
NC_000002.10:g.85632546T=	NCBI36
NG_011811.2:g.14623A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5987A=
ENST00000482662.2:n.4394A=
ENST00000685865.1:n.2346A=
ENST00000687250.1:n.2046A=
ENST00000687995.1:n.1861A=
ENST00000688205.1:c.*1102A=	ENSP00000509673.1:n.*1102A=
ENST00000688788.1:n.1748A=
ENST00000689276.1:c.1440A=	ENSP00000510012.1:p.Gln480=
ENST00000689576.1:c.*128A=	ENSP00000508712.1:n.*128A=
ENST00000690108.1:c.*1165A=	ENSP00000510617.1:n.*1165A=
ENST00000690468.1:c.*61A=	ENSP00000509078.1:n.*61A=
ENST00000690595.1:c.834A=	ENSP00000508979.1:p.Gln278=
ENST00000691348.1:c.*61A=	ENSP00000509369.1:n.*61A=
ENST00000691410.1:c.*1086A=	ENSP00000508479.1:n.*1086A=
ENST00000693287.1:c.825A=	ENSP00000510264.1:p.Gln275=
ENST00000693681.1:c.822A=	ENSP00000510789.1:p.Gln274=
ENST00000233838.9:c.1509A= MANE Select	ENSP00000233838.3:p.Gln503=
ENST00000233838.8:c.1509A=	ENSP00000233838.3:p.Gln503=
ENST00000430215.7:c.1338A=	ENSP00000408045.3:p.Gln446=
ENST00000465637.5:n.179-3908A=
NM_000821.5:c.1509A=	NP_000812.2:p.Gln503=
NM_000821.6:c.1509A=	NP_000812.2:p.Gln503=
NM_001142269.2:c.1338A=	NP_001135741.1:p.Gln446=
NM_001142269.3:c.1338A=	NP_001135741.1:p.Gln446=
XM_005264259.3:c.1509A=	XP_005264316.1:p.Gln503=
XM_011532764.1:c.687A=	XP_011531066.1:p.Gln229=
XM_011532765.1:c.687A=	XP_011531067.1:p.Gln229=
XR_939677.1:n.1422A=
XM_005264259.5:c.1509A=	XP_005264316.1:p.Gln503=
XM_011532764.3:c.687A=	XP_011531066.1:p.Gln229=
XM_011532765.3:c.687A=	XP_011531067.1:p.Gln229=
XM_017003803.2:c.1338A=	XP_016859292.1:p.Gln446=
XR_001738703.2:n.1422A=
NM_000821.7:c.1509A= MANE Select	NP_000812.2:p.Gln503=
NM_001142269.4:c.1338A=	NP_001135741.1:p.Gln446=