Canonical Allele Identifier: CA1266824951

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551972G= , CM000664.2:g.85551972G=	GRCh38
NC_000002.11:g.85779095G= , CM000664.1:g.85779095G=	GRCh37
NC_000002.10:g.85632606G=	NCBI36
NG_011811.2:g.14563C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5927C=
ENST00000482662.2:n.4334C=
ENST00000685865.1:n.2286C=
ENST00000687250.1:n.1986C=
ENST00000687995.1:n.1801C=
ENST00000688205.1:c.*1042C=	ENSP00000509673.1:n.*1042C=
ENST00000688788.1:n.1688C=
ENST00000689276.1:c.1380C=	ENSP00000510012.1:p.Asp460=
ENST00000689576.1:c.*68C=	ENSP00000508712.1:n.*68C=
ENST00000690108.1:c.*1105C=	ENSP00000510617.1:n.*1105C=
ENST00000690468.1:c.*1C=	ENSP00000509078.1:n.*1C=
ENST00000690595.1:c.774C=	ENSP00000508979.1:p.Asp258=
ENST00000691348.1:c.*1C=	ENSP00000509369.1:n.*1C=
ENST00000691410.1:c.*1026C=	ENSP00000508479.1:n.*1026C=
ENST00000693287.1:c.765C=	ENSP00000510264.1:p.Asp255=
ENST00000693681.1:c.762C=	ENSP00000510789.1:p.Asp254=
ENST00000233838.9:c.1449C= MANE Select	ENSP00000233838.3:p.Asp483=
ENST00000233838.8:c.1449C=	ENSP00000233838.3:p.Asp483=
ENST00000430215.7:c.1278C=	ENSP00000408045.3:p.Asp426=
ENST00000465637.5:n.179-3968C=
NM_000821.5:c.1449C=	NP_000812.2:p.Asp483=
NM_000821.6:c.1449C=	NP_000812.2:p.Asp483=
NM_001142269.2:c.1278C=	NP_001135741.1:p.Asp426=
NM_001142269.3:c.1278C=	NP_001135741.1:p.Asp426=
XM_005264259.3:c.1449C=	XP_005264316.1:p.Asp483=
XM_011532764.1:c.627C=	XP_011531066.1:p.Asp209=
XM_011532765.1:c.627C=	XP_011531067.1:p.Asp209=
XR_939677.1:n.1362C=
XM_005264259.5:c.1449C=	XP_005264316.1:p.Asp483=
XM_011532764.3:c.627C=	XP_011531066.1:p.Asp209=
XM_011532765.3:c.627C=	XP_011531067.1:p.Asp209=
XM_017003803.2:c.1278C=	XP_016859292.1:p.Asp426=
XR_001738703.2:n.1362C=
NM_000821.7:c.1449C= MANE Select	NP_000812.2:p.Asp483=
NM_001142269.4:c.1278C=	NP_001135741.1:p.Asp426=