Canonical Allele Identifier: CA413412323
Gene: ZC4H2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64921917T>C , CM000685.2:g.64921917T>C GRCh38
NC_000023.10:g.64141797T>C , CM000685.1:g.64141797T>C GRCh37
NC_000023.9:g.64058522T>C NCBI36
NG_021200.1:g.59617A>G
NG_021200.2:g.117828A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476032.2:c.56A>G ENSP00000515193.1:p.Glu19Gly
ENST00000492653.6:c.125A>G ENSP00000515192.1:p.Glu42Gly
ENST00000703133.1:c.*699A>G ENSP00000515188.1:n.*699A>G
ENST00000703136.1:c.*83A>G ENSP00000515190.1:n.*83A>G
ENST00000374839.8:c.125A>G MANE Select ENSP00000363972.3:p.Glu42Gly
ENST00000337990.2:c.56A>G ENSP00000338650.2:p.Glu19Gly
ENST00000374839.7:c.125A>G ENSP00000363972.3:p.Glu42Gly
ENST00000447788.6:c.125A>G ENSP00000399126.2:p.Glu42Gly
ENST00000476032.1:n.366A>G
ENST00000488608.5:n.281A>G
ENST00000488831.5:n.113A>G
ENST00000492653.5:n.221A>G
NM_001178032.2:c.56A>G NP_001171503.1:p.Glu19Gly
NM_001178033.2:c.125A>G NP_001171504.1:p.Glu42Gly
NM_001243804.1:c.56A>G NP_001230733.1:p.Glu19Gly
NM_018684.3:c.125A>G NP_061154.1:p.Glu42Gly
NR_045044.1:n.536A>G
NM_018684.4:c.125A>G MANE Select NP_061154.1:p.Glu42Gly
NM_001178032.3:c.56A>G NP_001171503.1:p.Glu19Gly
NM_001243804.2:c.56A>G NP_001230733.1:p.Glu19Gly
NR_045044.2:n.453A>G
NM_001178033.3:c.125A>G NP_001171504.1:p.Glu42Gly