Canonical Allele Identifier: CA1266824931

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551936G= , CM000664.2:g.85551936G=	GRCh38
NC_000002.11:g.85779059G= , CM000664.1:g.85779059G=	GRCh37
NC_000002.10:g.85632570G=	NCBI36
NG_011811.2:g.14599C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5963C=
ENST00000482662.2:n.4370C=
ENST00000685865.1:n.2322C=
ENST00000687250.1:n.2022C=
ENST00000687995.1:n.1837C=
ENST00000688205.1:c.*1078C=	ENSP00000509673.1:n.*1078C=
ENST00000688788.1:n.1724C=
ENST00000689276.1:c.1416C=	ENSP00000510012.1:p.Pro472=
ENST00000689576.1:c.*104C=	ENSP00000508712.1:n.*104C=
ENST00000690108.1:c.*1141C=	ENSP00000510617.1:n.*1141C=
ENST00000690468.1:c.*37C=	ENSP00000509078.1:n.*37C=
ENST00000690595.1:c.810C=	ENSP00000508979.1:p.Pro270=
ENST00000691348.1:c.*37C=	ENSP00000509369.1:n.*37C=
ENST00000691410.1:c.*1062C=	ENSP00000508479.1:n.*1062C=
ENST00000693287.1:c.801C=	ENSP00000510264.1:p.Pro267=
ENST00000693681.1:c.798C=	ENSP00000510789.1:p.Pro266=
ENST00000233838.9:c.1485C= MANE Select	ENSP00000233838.3:p.Pro495=
ENST00000233838.8:c.1485C=	ENSP00000233838.3:p.Pro495=
ENST00000430215.7:c.1314C=	ENSP00000408045.3:p.Pro438=
ENST00000465637.5:n.179-3932C=
NM_000821.5:c.1485C=	NP_000812.2:p.Pro495=
NM_000821.6:c.1485C=	NP_000812.2:p.Pro495=
NM_001142269.2:c.1314C=	NP_001135741.1:p.Pro438=
NM_001142269.3:c.1314C=	NP_001135741.1:p.Pro438=
XM_005264259.3:c.1485C=	XP_005264316.1:p.Pro495=
XM_011532764.1:c.663C=	XP_011531066.1:p.Pro221=
XM_011532765.1:c.663C=	XP_011531067.1:p.Pro221=
XR_939677.1:n.1398C=
XM_005264259.5:c.1485C=	XP_005264316.1:p.Pro495=
XM_011532764.3:c.663C=	XP_011531066.1:p.Pro221=
XM_011532765.3:c.663C=	XP_011531067.1:p.Pro221=
XM_017003803.2:c.1314C=	XP_016859292.1:p.Pro438=
XR_001738703.2:n.1398C=
NM_000821.7:c.1485C= MANE Select	NP_000812.2:p.Pro495=
NM_001142269.4:c.1314C=	NP_001135741.1:p.Pro438=