Canonical Allele Identifier: CA347484817
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551857T>A , CM000664.2:g.85551857T>A GRCh38
NC_000002.11:g.85778980T>A , CM000664.1:g.85778980T>A GRCh37
NC_000002.10:g.85632491T>A NCBI36
NG_011811.2:g.14678A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.6042A>T
ENST00000482662.2:n.4449A>T
ENST00000685865.1:n.2401A>T
ENST00000687250.1:n.2101A>T
ENST00000687995.1:n.1916A>T
ENST00000688205.1:c.*1157A>T ENSP00000509673.1:n.*1157A>T
ENST00000688788.1:n.1803A>T
ENST00000689276.1:c.1495A>T ENSP00000510012.1:p.Ser499Cys
ENST00000689576.1:c.*183A>T ENSP00000508712.1:n.*183A>T
ENST00000690108.1:c.*1220A>T ENSP00000510617.1:n.*1220A>T
ENST00000690468.1:c.*116A>T ENSP00000509078.1:n.*116A>T
ENST00000690595.1:c.889A>T ENSP00000508979.1:p.Ser297Cys
ENST00000691348.1:c.*116A>T ENSP00000509369.1:n.*116A>T
ENST00000691410.1:c.*1141A>T ENSP00000508479.1:n.*1141A>T
ENST00000693287.1:c.880A>T ENSP00000510264.1:p.Ser294Cys
ENST00000693681.1:c.877A>T ENSP00000510789.1:p.Ser293Cys
ENST00000233838.9:c.1564A>T MANE Select ENSP00000233838.3:p.Ser522Cys
ENST00000233838.8:c.1564A>T ENSP00000233838.3:p.Ser522Cys
ENST00000430215.7:c.1393A>T ENSP00000408045.3:p.Ser465Cys
ENST00000465637.5:n.179-3853A>T
NM_000821.5:c.1564A>T NP_000812.2:p.Ser522Cys
NM_000821.6:c.1564A>T NP_000812.2:p.Ser522Cys
NM_001142269.2:c.1393A>T NP_001135741.1:p.Ser465Cys
NM_001142269.3:c.1393A>T NP_001135741.1:p.Ser465Cys
XM_005264259.3:c.1564A>T XP_005264316.1:p.Ser522Cys
XM_011532764.1:c.742A>T XP_011531066.1:p.Ser248Cys
XM_011532765.1:c.742A>T XP_011531067.1:p.Ser248Cys
XR_939677.1:n.1477A>T
XM_005264259.5:c.1564A>T XP_005264316.1:p.Ser522Cys
XM_011532764.3:c.742A>T XP_011531066.1:p.Ser248Cys
XM_011532765.3:c.742A>T XP_011531067.1:p.Ser248Cys
XM_017003803.2:c.1393A>T XP_016859292.1:p.Ser465Cys
XR_001738703.2:n.1477A>T
NM_000821.7:c.1564A>T MANE Select NP_000812.2:p.Ser522Cys
NM_001142269.4:c.1393A>T NP_001135741.1:p.Ser465Cys