Canonical Allele Identifier: CA413411158

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137728G>A (hg19) ; chrX:g.64917848G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917848G>A , CM000685.2:g.64917848G>A	GRCh38
NC_000023.10:g.64137728G>A , CM000685.1:g.64137728G>A	GRCh37
NC_000023.9:g.64054453G>A	NCBI36
NG_021200.1:g.63686C>T
NG_021200.2:g.121897C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*234C>T	ENSP00000515192.1:n.*234C>T
ENST00000703133.1:c.*1184C>T	ENSP00000515188.1:n.*1184C>T
ENST00000703136.1:c.*568C>T	ENSP00000515190.1:n.*568C>T
ENST00000374839.8:c.610C>T MANE Select	ENSP00000363972.3:p.Pro204Ser
ENST00000337990.2:c.541C>T	ENSP00000338650.2:p.Pro181Ser
ENST00000374839.7:c.610C>T	ENSP00000363972.3:p.Pro204Ser
ENST00000447788.6:c.447C>T	ENSP00000399126.2:p.Ala149=
ENST00000488406.1:n.130C>T
ENST00000488608.5:n.2787C>T
ENST00000488831.5:n.598C>T
ENST00000492653.5:n.738C>T
NM_001178032.2:c.541C>T	NP_001171503.1:p.Pro181Ser
NM_001178033.2:c.447C>T	NP_001171504.1:p.Ala149=
NM_001243804.1:c.541C>T	NP_001230733.1:p.Pro181Ser
NM_018684.3:c.610C>T	NP_061154.1:p.Pro204Ser
NR_045044.1:n.1021C>T
NM_018684.4:c.610C>T MANE Select	NP_061154.1:p.Pro204Ser
NM_001178032.3:c.541C>T	NP_001171503.1:p.Pro181Ser
NM_001243804.2:c.541C>T	NP_001230733.1:p.Pro181Ser
NR_045044.2:n.938C>T
NM_001178033.3:c.447C>T	NP_001171504.1:p.Ala149=