Canonical Allele Identifier: CA2433764015

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921854A= , CM000685.2:g.64921854A=	GRCh38
NC_000023.10:g.64141734A= , CM000685.1:g.64141734A=	GRCh37
NC_000023.9:g.64058459A=	NCBI36
NG_021200.1:g.59680T=
NG_021200.2:g.117891T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.119T=	ENSP00000515193.1:p.Val40=
ENST00000492653.6:c.188T=	ENSP00000515192.1:p.Val63=
ENST00000703133.1:c.*762T=	ENSP00000515188.1:n.*762T=
ENST00000703136.1:c.*146T=	ENSP00000515190.1:n.*146T=
ENST00000374839.8:c.188T= MANE Select	ENSP00000363972.3:p.Val63=
ENST00000337990.2:c.119T=	ENSP00000338650.2:p.Val40=
ENST00000374839.7:c.188T=	ENSP00000363972.3:p.Val63=
ENST00000447788.6:c.188T=	ENSP00000399126.2:p.Val63=
ENST00000476032.1:n.429T=
ENST00000488608.5:n.344T=
ENST00000488831.5:n.176T=
ENST00000492653.5:n.284T=
NM_001178032.2:c.119T=	NP_001171503.1:p.Val40=
NM_001178033.2:c.188T=	NP_001171504.1:p.Val63=
NM_001243804.1:c.119T=	NP_001230733.1:p.Val40=
NM_018684.3:c.188T=	NP_061154.1:p.Val63=
NR_045044.1:n.599T=
NM_018684.4:c.188T= MANE Select	NP_061154.1:p.Val63=
NM_001178032.3:c.119T=	NP_001171503.1:p.Val40=
NM_001243804.2:c.119T=	NP_001230733.1:p.Val40=
NR_045044.2:n.516T=
NM_001178033.3:c.188T=	NP_001171504.1:p.Val63=