Canonical Allele Identifier: CA347484918
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551901A>T , CM000664.2:g.85551901A>T GRCh38
NC_000002.11:g.85779024A>T , CM000664.1:g.85779024A>T GRCh37
NC_000002.10:g.85632535A>T NCBI36
NG_011811.2:g.14634T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5998T>A
ENST00000482662.2:n.4405T>A
ENST00000685865.1:n.2357T>A
ENST00000687250.1:n.2057T>A
ENST00000687995.1:n.1872T>A
ENST00000688205.1:c.*1113T>A ENSP00000509673.1:n.*1113T>A
ENST00000688788.1:n.1759T>A
ENST00000689276.1:c.1451T>A ENSP00000510012.1:p.Met484Lys
ENST00000689576.1:c.*139T>A ENSP00000508712.1:n.*139T>A
ENST00000690108.1:c.*1176T>A ENSP00000510617.1:n.*1176T>A
ENST00000690468.1:c.*72T>A ENSP00000509078.1:n.*72T>A
ENST00000690595.1:c.845T>A ENSP00000508979.1:p.Met282Lys
ENST00000691348.1:c.*72T>A ENSP00000509369.1:n.*72T>A
ENST00000691410.1:c.*1097T>A ENSP00000508479.1:n.*1097T>A
ENST00000693287.1:c.836T>A ENSP00000510264.1:p.Met279Lys
ENST00000693681.1:c.833T>A ENSP00000510789.1:p.Met278Lys
ENST00000233838.9:c.1520T>A MANE Select ENSP00000233838.3:p.Met507Lys
ENST00000233838.8:c.1520T>A ENSP00000233838.3:p.Met507Lys
ENST00000430215.7:c.1349T>A ENSP00000408045.3:p.Met450Lys
ENST00000465637.5:n.179-3897T>A
NM_000821.5:c.1520T>A NP_000812.2:p.Met507Lys
NM_000821.6:c.1520T>A NP_000812.2:p.Met507Lys
NM_001142269.2:c.1349T>A NP_001135741.1:p.Met450Lys
NM_001142269.3:c.1349T>A NP_001135741.1:p.Met450Lys
XM_005264259.3:c.1520T>A XP_005264316.1:p.Met507Lys
XM_011532764.1:c.698T>A XP_011531066.1:p.Met233Lys
XM_011532765.1:c.698T>A XP_011531067.1:p.Met233Lys
XR_939677.1:n.1433T>A
XM_005264259.5:c.1520T>A XP_005264316.1:p.Met507Lys
XM_011532764.3:c.698T>A XP_011531066.1:p.Met233Lys
XM_011532765.3:c.698T>A XP_011531067.1:p.Met233Lys
XM_017003803.2:c.1349T>A XP_016859292.1:p.Met450Lys
XR_001738703.2:n.1433T>A
NM_000821.7:c.1520T>A MANE Select NP_000812.2:p.Met507Lys
NM_001142269.4:c.1349T>A NP_001135741.1:p.Met450Lys