Canonical Allele Identifier: CA347485055
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551965C>T , CM000664.2:g.85551965C>T GRCh38
NC_000002.11:g.85779088C>T , CM000664.1:g.85779088C>T GRCh37
NC_000002.10:g.85632599C>T NCBI36
NG_011811.2:g.14570G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5934G>A
ENST00000482662.2:n.4341G>A
ENST00000685865.1:n.2293G>A
ENST00000687250.1:n.1993G>A
ENST00000687995.1:n.1808G>A
ENST00000688205.1:c.*1049G>A ENSP00000509673.1:n.*1049G>A
ENST00000688788.1:n.1695G>A
ENST00000689276.1:c.1387G>A ENSP00000510012.1:p.Val463Met
ENST00000689576.1:c.*75G>A ENSP00000508712.1:n.*75G>A
ENST00000690108.1:c.*1112G>A ENSP00000510617.1:n.*1112G>A
ENST00000690468.1:c.*8G>A ENSP00000509078.1:n.*8G>A
ENST00000690595.1:c.781G>A ENSP00000508979.1:p.Val261Met
ENST00000691348.1:c.*8G>A ENSP00000509369.1:n.*8G>A
ENST00000691410.1:c.*1033G>A ENSP00000508479.1:n.*1033G>A
ENST00000693287.1:c.772G>A ENSP00000510264.1:p.Val258Met
ENST00000693681.1:c.769G>A ENSP00000510789.1:p.Val257Met
ENST00000233838.9:c.1456G>A MANE Select ENSP00000233838.3:p.Val486Met
ENST00000233838.8:c.1456G>A ENSP00000233838.3:p.Val486Met
ENST00000430215.7:c.1285G>A ENSP00000408045.3:p.Val429Met
ENST00000465637.5:n.179-3961G>A
NM_000821.5:c.1456G>A NP_000812.2:p.Val486Met
NM_000821.6:c.1456G>A NP_000812.2:p.Val486Met
NM_001142269.2:c.1285G>A NP_001135741.1:p.Val429Met
NM_001142269.3:c.1285G>A NP_001135741.1:p.Val429Met
XM_005264259.3:c.1456G>A XP_005264316.1:p.Val486Met
XM_011532764.1:c.634G>A XP_011531066.1:p.Val212Met
XM_011532765.1:c.634G>A XP_011531067.1:p.Val212Met
XR_939677.1:n.1369G>A
XM_005264259.5:c.1456G>A XP_005264316.1:p.Val486Met
XM_011532764.3:c.634G>A XP_011531066.1:p.Val212Met
XM_011532765.3:c.634G>A XP_011531067.1:p.Val212Met
XM_017003803.2:c.1285G>A XP_016859292.1:p.Val429Met
XR_001738703.2:n.1369G>A
NM_000821.7:c.1456G>A MANE Select NP_000812.2:p.Val486Met
NM_001142269.4:c.1285G>A NP_001135741.1:p.Val429Met