Canonical Allele Identifier: CA1266825499

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553234G= , CM000664.2:g.85553234G=	GRCh38
NC_000002.11:g.85780357G= , CM000664.1:g.85780357G=	GRCh37
NC_000002.10:g.85633868G=	NCBI36
NG_011811.2:g.13301C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5197C=
ENST00000482662.2:n.3604C=
ENST00000685865.1:n.1556C=
ENST00000687250.1:n.1256C=
ENST00000687995.1:n.1505C=
ENST00000688205.1:c.*746C=	ENSP00000509673.1:n.*746C=
ENST00000688788.1:n.1392C=
ENST00000689276.1:c.1084C=	ENSP00000510012.1:p.Gln362=
ENST00000689576.1:c.1153C=	ENSP00000508712.1:p.Gln385=
ENST00000690108.1:c.*809C=	ENSP00000510617.1:n.*809C=
ENST00000690468.1:c.874C=	ENSP00000509078.1:p.Gln292=
ENST00000690595.1:c.478C=	ENSP00000508979.1:p.Gln160=
ENST00000691348.1:c.982C=	ENSP00000509369.1:p.Gln328=
ENST00000691410.1:c.*730C=	ENSP00000508479.1:n.*730C=
ENST00000693287.1:c.469C=	ENSP00000510264.1:p.Gln157=
ENST00000693681.1:c.466C=	ENSP00000510789.1:p.Gln156=
ENST00000233838.9:c.1153C= MANE Select	ENSP00000233838.3:p.Gln385=
ENST00000233838.8:c.1153C=	ENSP00000233838.3:p.Gln385=
ENST00000430215.7:c.982C=	ENSP00000408045.3:p.Gln328=
ENST00000465637.5:n.179-5230C=
ENST00000473665.1:n.646C=
ENST00000482662.1:n.570C=
NM_000821.5:c.1153C=	NP_000812.2:p.Gln385=
NM_000821.6:c.1153C=	NP_000812.2:p.Gln385=
NM_001142269.2:c.982C=	NP_001135741.1:p.Gln328=
NM_001142269.3:c.982C=	NP_001135741.1:p.Gln328=
XM_005264259.3:c.1153C=	XP_005264316.1:p.Gln385=
XM_011532764.1:c.331C=	XP_011531066.1:p.Gln111=
XM_011532765.1:c.331C=	XP_011531067.1:p.Gln111=
XR_939677.1:n.1218C=
XM_005264259.5:c.1153C=	XP_005264316.1:p.Gln385=
XM_011532764.3:c.331C=	XP_011531066.1:p.Gln111=
XM_011532765.3:c.331C=	XP_011531067.1:p.Gln111=
XM_017003803.2:c.982C=	XP_016859292.1:p.Gln328=
XR_001738703.2:n.1218C=
NM_000821.7:c.1153C= MANE Select	NP_000812.2:p.Gln385=
NM_001142269.4:c.982C=	NP_001135741.1:p.Gln328=