Canonical Allele Identifier: CA516907192

Gene: ZC4H2

Linked Data

• gnomAD v4: X-64921850-C-T
• MyVariant Identifiers: chrX:g.64141730C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921850C>T , CM000685.2:g.64921850C>T	GRCh38
NC_000023.10:g.64141730C>T , CM000685.1:g.64141730C>T	GRCh37
NC_000023.9:g.64058455C>T	NCBI36
NG_021200.1:g.59684G>A
NG_021200.2:g.117895G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000476032.2:c.123G>A	ENSP00000515193.1:p.Glu41=
ENST00000492653.6:c.192G>A	ENSP00000515192.1:p.Glu64=
ENST00000703133.1:c.*766G>A	ENSP00000515188.1:n.*766G>A
ENST00000703136.1:c.*150G>A	ENSP00000515190.1:n.*150G>A
ENST00000374839.8:c.192G>A MANE Select	ENSP00000363972.3:p.Glu64=
ENST00000337990.2:c.123G>A	ENSP00000338650.2:p.Glu41=
ENST00000374839.7:c.192G>A	ENSP00000363972.3:p.Glu64=
ENST00000447788.6:c.192G>A	ENSP00000399126.2:p.Glu64=
ENST00000476032.1:n.433G>A
ENST00000488608.5:n.348G>A
ENST00000488831.5:n.180G>A
ENST00000492653.5:n.288G>A
NM_001178032.2:c.123G>A	NP_001171503.1:p.Glu41=
NM_001178033.2:c.192G>A	NP_001171504.1:p.Glu64=
NM_001243804.1:c.123G>A	NP_001230733.1:p.Glu41=
NM_018684.3:c.192G>A	NP_061154.1:p.Glu64=
NR_045044.1:n.603G>A
NM_018684.4:c.192G>A MANE Select	NP_061154.1:p.Glu64=
NM_001178032.3:c.123G>A	NP_001171503.1:p.Glu41=
NM_001243804.2:c.123G>A	NP_001230733.1:p.Glu41=
NR_045044.2:n.520G>A
NM_001178033.3:c.192G>A	NP_001171504.1:p.Glu64=