Canonical Allele Identifier: CA2433762461

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917822G= , CM000685.2:g.64917822G=	GRCh38
NC_000023.10:g.64137702G= , CM000685.1:g.64137702G=	GRCh37
NC_000023.9:g.64054427G=	NCBI36
NG_021200.1:g.63712C=
NG_021200.2:g.121923C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492653.6:c.*260C=	ENSP00000515192.1:n.*260C=
ENST00000703133.1:c.*1210C=	ENSP00000515188.1:n.*1210C=
ENST00000703136.1:c.*594C=	ENSP00000515190.1:n.*594C=
ENST00000374839.8:c.636C= MANE Select	ENSP00000363972.3:p.Ser212=
ENST00000337990.2:c.567C=	ENSP00000338650.2:p.Ser189=
ENST00000374839.7:c.636C=	ENSP00000363972.3:p.Ser212=
ENST00000447788.6:c.473C=	ENSP00000399126.2:p.Pro158=
ENST00000488406.1:n.156C=
ENST00000488608.5:n.2813C=
ENST00000492653.5:n.764C=
NM_001178032.2:c.567C=	NP_001171503.1:p.Ser189=
NM_001178033.2:c.473C=	NP_001171504.1:p.Pro158=
NM_001243804.1:c.567C=	NP_001230733.1:p.Ser189=
NM_018684.3:c.636C=	NP_061154.1:p.Ser212=
NR_045044.1:n.1047C=
NM_018684.4:c.636C= MANE Select	NP_061154.1:p.Ser212=
NM_001178032.3:c.567C=	NP_001171503.1:p.Ser189=
NM_001243804.2:c.567C=	NP_001230733.1:p.Ser189=
NR_045044.2:n.964C=
NM_001178033.3:c.473C=	NP_001171504.1:p.Pro158=