Canonical Allele Identifier: CA516907199

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64141739G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921859G>T , CM000685.2:g.64921859G>T	GRCh38
NC_000023.10:g.64141739G>T , CM000685.1:g.64141739G>T	GRCh37
NC_000023.9:g.64058464G>T	NCBI36
NG_021200.1:g.59675C>A
NG_021200.2:g.117886C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000476032.2:c.114C>A	ENSP00000515193.1:p.Ala38=
ENST00000492653.6:c.183C>A	ENSP00000515192.1:p.Ala61=
ENST00000703133.1:c.*757C>A	ENSP00000515188.1:n.*757C>A
ENST00000703136.1:c.*141C>A	ENSP00000515190.1:n.*141C>A
ENST00000374839.8:c.183C>A MANE Select	ENSP00000363972.3:p.Ala61=
ENST00000337990.2:c.114C>A	ENSP00000338650.2:p.Ala38=
ENST00000374839.7:c.183C>A	ENSP00000363972.3:p.Ala61=
ENST00000447788.6:c.183C>A	ENSP00000399126.2:p.Ala61=
ENST00000476032.1:n.424C>A
ENST00000488608.5:n.339C>A
ENST00000488831.5:n.171C>A
ENST00000492653.5:n.279C>A
NM_001178032.2:c.114C>A	NP_001171503.1:p.Ala38=
NM_001178033.2:c.183C>A	NP_001171504.1:p.Ala61=
NM_001243804.1:c.114C>A	NP_001230733.1:p.Ala38=
NM_018684.3:c.183C>A	NP_061154.1:p.Ala61=
NR_045044.1:n.594C>A
NM_018684.4:c.183C>A MANE Select	NP_061154.1:p.Ala61=
NM_001178032.3:c.114C>A	NP_001171503.1:p.Ala38=
NM_001243804.2:c.114C>A	NP_001230733.1:p.Ala38=
NR_045044.2:n.511C>A
NM_001178033.3:c.183C>A	NP_001171504.1:p.Ala61=