Canonical Allele Identifier: CA413412332

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64141800T>C (hg19) ; chrX:g.64921920T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921920T>C , CM000685.2:g.64921920T>C	GRCh38
NC_000023.10:g.64141800T>C , CM000685.1:g.64141800T>C	GRCh37
NC_000023.9:g.64058525T>C	NCBI36
NG_021200.1:g.59614A>G
NG_021200.2:g.117825A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.53A>G	ENSP00000515193.1:p.Glu18Gly
ENST00000492653.6:c.122A>G	ENSP00000515192.1:p.Glu41Gly
ENST00000703133.1:c.*696A>G	ENSP00000515188.1:n.*696A>G
ENST00000703136.1:c.*80A>G	ENSP00000515190.1:n.*80A>G
ENST00000374839.8:c.122A>G MANE Select	ENSP00000363972.3:p.Glu41Gly
ENST00000337990.2:c.53A>G	ENSP00000338650.2:p.Glu18Gly
ENST00000374839.7:c.122A>G	ENSP00000363972.3:p.Glu41Gly
ENST00000447788.6:c.122A>G	ENSP00000399126.2:p.Glu41Gly
ENST00000476032.1:n.363A>G
ENST00000488608.5:n.278A>G
ENST00000488831.5:n.110A>G
ENST00000492653.5:n.218A>G
NM_001178032.2:c.53A>G	NP_001171503.1:p.Glu18Gly
NM_001178033.2:c.122A>G	NP_001171504.1:p.Glu41Gly
NM_001243804.1:c.53A>G	NP_001230733.1:p.Glu18Gly
NM_018684.3:c.122A>G	NP_061154.1:p.Glu41Gly
NR_045044.1:n.533A>G
NM_018684.4:c.122A>G MANE Select	NP_061154.1:p.Glu41Gly
NM_001178032.3:c.53A>G	NP_001171503.1:p.Glu18Gly
NM_001243804.2:c.53A>G	NP_001230733.1:p.Glu18Gly
NR_045044.2:n.450A>G
NM_001178033.3:c.122A>G	NP_001171504.1:p.Glu41Gly