Canonical Allele Identifier: CA516907222

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64141789G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921909G>A , CM000685.2:g.64921909G>A	GRCh38
NC_000023.10:g.64141789G>A , CM000685.1:g.64141789G>A	GRCh37
NC_000023.9:g.64058514G>A	NCBI36
NG_021200.1:g.59625C>T
NG_021200.2:g.117836C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.64C>T	ENSP00000515193.1:p.Leu22=
ENST00000492653.6:c.133C>T	ENSP00000515192.1:p.Leu45=
ENST00000703133.1:c.*707C>T	ENSP00000515188.1:n.*707C>T
ENST00000703136.1:c.*91C>T	ENSP00000515190.1:n.*91C>T
ENST00000374839.8:c.133C>T MANE Select	ENSP00000363972.3:p.Leu45=
ENST00000337990.2:c.64C>T	ENSP00000338650.2:p.Leu22=
ENST00000374839.7:c.133C>T	ENSP00000363972.3:p.Leu45=
ENST00000447788.6:c.133C>T	ENSP00000399126.2:p.Leu45=
ENST00000476032.1:n.374C>T
ENST00000488608.5:n.289C>T
ENST00000488831.5:n.121C>T
ENST00000492653.5:n.229C>T
NM_001178032.2:c.64C>T	NP_001171503.1:p.Leu22=
NM_001178033.2:c.133C>T	NP_001171504.1:p.Leu45=
NM_001243804.1:c.64C>T	NP_001230733.1:p.Leu22=
NM_018684.3:c.133C>T	NP_061154.1:p.Leu45=
NR_045044.1:n.544C>T
NM_018684.4:c.133C>T MANE Select	NP_061154.1:p.Leu45=
NM_001178032.3:c.64C>T	NP_001171503.1:p.Leu22=
NM_001243804.2:c.64C>T	NP_001230733.1:p.Leu22=
NR_045044.2:n.461C>T
NM_001178033.3:c.133C>T	NP_001171504.1:p.Leu45=