Canonical Allele Identifier: CA2433762469

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917843A= , CM000685.2:g.64917843A=	GRCh38
NC_000023.10:g.64137723A= , CM000685.1:g.64137723A=	GRCh37
NC_000023.9:g.64054448A=	NCBI36
NG_021200.1:g.63691T=
NG_021200.2:g.121902T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*239T=	ENSP00000515192.1:n.*239T=
ENST00000703133.1:c.*1189T=	ENSP00000515188.1:n.*1189T=
ENST00000703136.1:c.*573T=	ENSP00000515190.1:n.*573T=
ENST00000374839.8:c.615T= MANE Select	ENSP00000363972.3:p.Leu205=
ENST00000337990.2:c.546T=	ENSP00000338650.2:p.Leu182=
ENST00000374839.7:c.615T=	ENSP00000363972.3:p.Leu205=
ENST00000447788.6:c.452T=	ENSP00000399126.2:p.Phe151=
ENST00000488406.1:n.135T=
ENST00000488608.5:n.2792T=
ENST00000488831.5:n.603T=
ENST00000492653.5:n.743T=
NM_001178032.2:c.546T=	NP_001171503.1:p.Leu182=
NM_001178033.2:c.452T=	NP_001171504.1:p.Phe151=
NM_001243804.1:c.546T=	NP_001230733.1:p.Leu182=
NM_018684.3:c.615T=	NP_061154.1:p.Leu205=
NR_045044.1:n.1026T=
NM_018684.4:c.615T= MANE Select	NP_061154.1:p.Leu205=
NM_001178032.3:c.546T=	NP_001171503.1:p.Leu182=
NM_001243804.2:c.546T=	NP_001230733.1:p.Leu182=
NR_045044.2:n.943T=
NM_001178033.3:c.452T=	NP_001171504.1:p.Phe151=