Canonical Allele Identifier: CA1266825417

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553054G= , CM000664.2:g.85553054G=	GRCh38
NC_000002.11:g.85780177G= , CM000664.1:g.85780177G=	GRCh37
NC_000002.10:g.85633688G=	NCBI36
NG_011811.2:g.13481C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5216C=
ENST00000482662.2:n.3623C=
ENST00000685865.1:n.1575C=
ENST00000687250.1:n.1275C=
ENST00000687995.1:n.1524C=
ENST00000688205.1:c.*765C=	ENSP00000509673.1:n.*765C=
ENST00000688788.1:n.1411C=
ENST00000689276.1:c.1103C=	ENSP00000510012.1:p.Thr368=
ENST00000689576.1:c.1172C=	ENSP00000508712.1:p.Thr391=
ENST00000690108.1:c.*828C=	ENSP00000510617.1:n.*828C=
ENST00000690468.1:c.893C=	ENSP00000509078.1:p.Thr298=
ENST00000690595.1:c.497C=	ENSP00000508979.1:p.Thr166=
ENST00000691348.1:c.1001C=	ENSP00000509369.1:p.Thr334=
ENST00000691410.1:c.*749C=	ENSP00000508479.1:n.*749C=
ENST00000693287.1:c.488C=	ENSP00000510264.1:p.Thr163=
ENST00000693681.1:c.485C=	ENSP00000510789.1:p.Thr162=
ENST00000233838.9:c.1172C= MANE Select	ENSP00000233838.3:p.Thr391=
ENST00000233838.8:c.1172C=	ENSP00000233838.3:p.Thr391=
ENST00000430215.7:c.1001C=	ENSP00000408045.3:p.Thr334=
ENST00000465637.5:n.179-5050C=
ENST00000473665.1:n.665C=
ENST00000482662.1:n.589C=
NM_000821.5:c.1172C=	NP_000812.2:p.Thr391=
NM_000821.6:c.1172C=	NP_000812.2:p.Thr391=
NM_001142269.2:c.1001C=	NP_001135741.1:p.Thr334=
NM_001142269.3:c.1001C=	NP_001135741.1:p.Thr334=
XM_005264259.3:c.1172C=	XP_005264316.1:p.Thr391=
XM_011532764.1:c.350C=	XP_011531066.1:p.Thr117=
XM_011532765.1:c.350C=	XP_011531067.1:p.Thr117=
XR_939677.1:n.1237C=
XM_005264259.5:c.1172C=	XP_005264316.1:p.Thr391=
XM_011532764.3:c.350C=	XP_011531066.1:p.Thr117=
XM_011532765.3:c.350C=	XP_011531067.1:p.Thr117=
XM_017003803.2:c.1001C=	XP_016859292.1:p.Thr334=
XR_001738703.2:n.1237C=
NM_000821.7:c.1172C= MANE Select	NP_000812.2:p.Thr391=
NM_001142269.4:c.1001C=	NP_001135741.1:p.Thr334=