Canonical Allele Identifier: CA347484867
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551877T>C , CM000664.2:g.85551877T>C GRCh38
NC_000002.11:g.85779000T>C , CM000664.1:g.85779000T>C GRCh37
NC_000002.10:g.85632511T>C NCBI36
NG_011811.2:g.14658A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.6022A>G
ENST00000482662.2:n.4429A>G
ENST00000685865.1:n.2381A>G
ENST00000687250.1:n.2081A>G
ENST00000687995.1:n.1896A>G
ENST00000688205.1:c.*1137A>G ENSP00000509673.1:n.*1137A>G
ENST00000688788.1:n.1783A>G
ENST00000689276.1:c.1475A>G ENSP00000510012.1:p.Lys492Arg
ENST00000689576.1:c.*163A>G ENSP00000508712.1:n.*163A>G
ENST00000690108.1:c.*1200A>G ENSP00000510617.1:n.*1200A>G
ENST00000690468.1:c.*96A>G ENSP00000509078.1:n.*96A>G
ENST00000690595.1:c.869A>G ENSP00000508979.1:p.Lys290Arg
ENST00000691348.1:c.*96A>G ENSP00000509369.1:n.*96A>G
ENST00000691410.1:c.*1121A>G ENSP00000508479.1:n.*1121A>G
ENST00000693287.1:c.860A>G ENSP00000510264.1:p.Lys287Arg
ENST00000693681.1:c.857A>G ENSP00000510789.1:p.Lys286Arg
ENST00000233838.9:c.1544A>G MANE Select ENSP00000233838.3:p.Lys515Arg
ENST00000233838.8:c.1544A>G ENSP00000233838.3:p.Lys515Arg
ENST00000430215.7:c.1373A>G ENSP00000408045.3:p.Lys458Arg
ENST00000465637.5:n.179-3873A>G
NM_000821.5:c.1544A>G NP_000812.2:p.Lys515Arg
NM_000821.6:c.1544A>G NP_000812.2:p.Lys515Arg
NM_001142269.2:c.1373A>G NP_001135741.1:p.Lys458Arg
NM_001142269.3:c.1373A>G NP_001135741.1:p.Lys458Arg
XM_005264259.3:c.1544A>G XP_005264316.1:p.Lys515Arg
XM_011532764.1:c.722A>G XP_011531066.1:p.Lys241Arg
XM_011532765.1:c.722A>G XP_011531067.1:p.Lys241Arg
XR_939677.1:n.1457A>G
XM_005264259.5:c.1544A>G XP_005264316.1:p.Lys515Arg
XM_011532764.3:c.722A>G XP_011531066.1:p.Lys241Arg
XM_011532765.3:c.722A>G XP_011531067.1:p.Lys241Arg
XM_017003803.2:c.1373A>G XP_016859292.1:p.Lys458Arg
XR_001738703.2:n.1457A>G
NM_000821.7:c.1544A>G MANE Select NP_000812.2:p.Lys515Arg
NM_001142269.4:c.1373A>G NP_001135741.1:p.Lys458Arg