Canonical Allele Identifier: CA516907217
Gene: ZC4H2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.64141781T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64921901T>C , CM000685.2:g.64921901T>C GRCh38
NC_000023.10:g.64141781T>C , CM000685.1:g.64141781T>C GRCh37
NC_000023.9:g.64058506T>C NCBI36
NG_021200.1:g.59633A>G
NG_021200.2:g.117844A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476032.2:c.72A>G ENSP00000515193.1:p.Glu24=
ENST00000492653.6:c.141A>G ENSP00000515192.1:p.Glu47=
ENST00000703133.1:c.*715A>G ENSP00000515188.1:n.*715A>G
ENST00000703136.1:c.*99A>G ENSP00000515190.1:n.*99A>G
ENST00000374839.8:c.141A>G MANE Select ENSP00000363972.3:p.Glu47=
ENST00000337990.2:c.72A>G ENSP00000338650.2:p.Glu24=
ENST00000374839.7:c.141A>G ENSP00000363972.3:p.Glu47=
ENST00000447788.6:c.141A>G ENSP00000399126.2:p.Glu47=
ENST00000476032.1:n.382A>G
ENST00000488608.5:n.297A>G
ENST00000488831.5:n.129A>G
ENST00000492653.5:n.237A>G
NM_001178032.2:c.72A>G NP_001171503.1:p.Glu24=
NM_001178033.2:c.141A>G NP_001171504.1:p.Glu47=
NM_001243804.1:c.72A>G NP_001230733.1:p.Glu24=
NM_018684.3:c.141A>G NP_061154.1:p.Glu47=
NR_045044.1:n.552A>G
NM_018684.4:c.141A>G MANE Select NP_061154.1:p.Glu47=
NM_001178032.3:c.72A>G NP_001171503.1:p.Glu24=
NM_001243804.2:c.72A>G NP_001230733.1:p.Glu24=
NR_045044.2:n.469A>G
NM_001178033.3:c.141A>G NP_001171504.1:p.Glu47=