Canonical Allele Identifier: CA2433764028

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921910G= , CM000685.2:g.64921910G=	GRCh38
NC_000023.10:g.64141790G= , CM000685.1:g.64141790G=	GRCh37
NC_000023.9:g.64058515G=	NCBI36
NG_021200.1:g.59624C=
NG_021200.2:g.117835C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.63C=	ENSP00000515193.1:p.His21=
ENST00000492653.6:c.132C=	ENSP00000515192.1:p.His44=
ENST00000703133.1:c.*706C=	ENSP00000515188.1:n.*706C=
ENST00000703136.1:c.*90C=	ENSP00000515190.1:n.*90C=
ENST00000374839.8:c.132C= MANE Select	ENSP00000363972.3:p.His44=
ENST00000337990.2:c.63C=	ENSP00000338650.2:p.His21=
ENST00000374839.7:c.132C=	ENSP00000363972.3:p.His44=
ENST00000447788.6:c.132C=	ENSP00000399126.2:p.His44=
ENST00000476032.1:n.373C=
ENST00000488608.5:n.288C=
ENST00000488831.5:n.120C=
ENST00000492653.5:n.228C=
NM_001178032.2:c.63C=	NP_001171503.1:p.His21=
NM_001178033.2:c.132C=	NP_001171504.1:p.His44=
NM_001243804.1:c.63C=	NP_001230733.1:p.His21=
NM_018684.3:c.132C=	NP_061154.1:p.His44=
NR_045044.1:n.543C=
NM_018684.4:c.132C= MANE Select	NP_061154.1:p.His44=
NM_001178032.3:c.63C=	NP_001171503.1:p.His21=
NM_001243804.2:c.63C=	NP_001230733.1:p.His21=
NR_045044.2:n.460C=
NM_001178033.3:c.132C=	NP_001171504.1:p.His44=