Canonical Allele Identifier: CA1266824902
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551856C= , CM000664.2:g.85551856C= GRCh38
NC_000002.11:g.85778979C= , CM000664.1:g.85778979C= GRCh37
NC_000002.10:g.85632490C= NCBI36
NG_011811.2:g.14679G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.6043G=
ENST00000482662.2:n.4450G=
ENST00000685865.1:n.2402G=
ENST00000687250.1:n.2102G=
ENST00000687995.1:n.1917G=
ENST00000688205.1:c.*1158G= ENSP00000509673.1:n.*1158G=
ENST00000688788.1:n.1804G=
ENST00000689276.1:c.1496G= ENSP00000510012.1:p.Ser499=
ENST00000689576.1:c.*184G= ENSP00000508712.1:n.*184G=
ENST00000690108.1:c.*1221G= ENSP00000510617.1:n.*1221G=
ENST00000690468.1:c.*117G= ENSP00000509078.1:n.*117G=
ENST00000690595.1:c.890G= ENSP00000508979.1:p.Ser297=
ENST00000691348.1:c.*117G= ENSP00000509369.1:n.*117G=
ENST00000691410.1:c.*1142G= ENSP00000508479.1:n.*1142G=
ENST00000693287.1:c.881G= ENSP00000510264.1:p.Ser294=
ENST00000693681.1:c.878G= ENSP00000510789.1:p.Ser293=
ENST00000233838.9:c.1565G= MANE Select ENSP00000233838.3:p.Ser522=
ENST00000233838.8:c.1565G= ENSP00000233838.3:p.Ser522=
ENST00000430215.7:c.1394G= ENSP00000408045.3:p.Ser465=
ENST00000465637.5:n.179-3852G=
NM_000821.5:c.1565G= NP_000812.2:p.Ser522=
NM_000821.6:c.1565G= NP_000812.2:p.Ser522=
NM_001142269.2:c.1394G= NP_001135741.1:p.Ser465=
NM_001142269.3:c.1394G= NP_001135741.1:p.Ser465=
XM_005264259.3:c.1565G= XP_005264316.1:p.Ser522=
XM_011532764.1:c.743G= XP_011531066.1:p.Ser248=
XM_011532765.1:c.743G= XP_011531067.1:p.Ser248=
XR_939677.1:n.1478G=
XM_005264259.5:c.1565G= XP_005264316.1:p.Ser522=
XM_011532764.3:c.743G= XP_011531066.1:p.Ser248=
XM_011532765.3:c.743G= XP_011531067.1:p.Ser248=
XM_017003803.2:c.1394G= XP_016859292.1:p.Ser465=
XR_001738703.2:n.1478G=
NM_000821.7:c.1565G= MANE Select NP_000812.2:p.Ser522=
NM_001142269.4:c.1394G= NP_001135741.1:p.Ser465=