Canonical Allele Identifier: CA2433762468

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917841C= , CM000685.2:g.64917841C=	GRCh38
NC_000023.10:g.64137721C= , CM000685.1:g.64137721C=	GRCh37
NC_000023.9:g.64054446C=	NCBI36
NG_021200.1:g.63693G=
NG_021200.2:g.121904G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*241G=	ENSP00000515192.1:n.*241G=
ENST00000703133.1:c.*1191G=	ENSP00000515188.1:n.*1191G=
ENST00000703136.1:c.*575G=	ENSP00000515190.1:n.*575G=
ENST00000374839.8:c.617G= MANE Select	ENSP00000363972.3:p.Cys206=
ENST00000337990.2:c.548G=	ENSP00000338650.2:p.Cys183=
ENST00000374839.7:c.617G=	ENSP00000363972.3:p.Cys206=
ENST00000447788.6:c.454G=	ENSP00000399126.2:p.Ala152=
ENST00000488406.1:n.137G=
ENST00000488608.5:n.2794G=
ENST00000488831.5:n.605G=
ENST00000492653.5:n.745G=
NM_001178032.2:c.548G=	NP_001171503.1:p.Cys183=
NM_001178033.2:c.454G=	NP_001171504.1:p.Ala152=
NM_001243804.1:c.548G=	NP_001230733.1:p.Cys183=
NM_018684.3:c.617G=	NP_061154.1:p.Cys206=
NR_045044.1:n.1028G=
NM_018684.4:c.617G= MANE Select	NP_061154.1:p.Cys206=
NM_001178032.3:c.548G=	NP_001171503.1:p.Cys183=
NM_001243804.2:c.548G=	NP_001230733.1:p.Cys183=
NR_045044.2:n.945G=
NM_001178033.3:c.454G=	NP_001171504.1:p.Ala152=