Canonical Allele Identifier: CA2433762471

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917852T= , CM000685.2:g.64917852T=	GRCh38
NC_000023.10:g.64137732T= , CM000685.1:g.64137732T=	GRCh37
NC_000023.9:g.64054457T=	NCBI36
NG_021200.1:g.63682A=
NG_021200.2:g.121893A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*230A=	ENSP00000515192.1:n.*230A=
ENST00000703133.1:c.*1180A=	ENSP00000515188.1:n.*1180A=
ENST00000703136.1:c.*564A=	ENSP00000515190.1:n.*564A=
ENST00000374839.8:c.606A= MANE Select	ENSP00000363972.3:p.Ile202=
ENST00000337990.2:c.537A=	ENSP00000338650.2:p.Ile179=
ENST00000374839.7:c.606A=	ENSP00000363972.3:p.Ile202=
ENST00000447788.6:c.443A=	ENSP00000399126.2:p.Tyr148=
ENST00000488406.1:n.126A=
ENST00000488608.5:n.2783A=
ENST00000488831.5:n.594A=
ENST00000492653.5:n.734A=
NM_001178032.2:c.537A=	NP_001171503.1:p.Ile179=
NM_001178033.2:c.443A=	NP_001171504.1:p.Tyr148=
NM_001243804.1:c.537A=	NP_001230733.1:p.Ile179=
NM_018684.3:c.606A=	NP_061154.1:p.Ile202=
NR_045044.1:n.1017A=
NM_018684.4:c.606A= MANE Select	NP_061154.1:p.Ile202=
NM_001178032.3:c.537A=	NP_001171503.1:p.Ile179=
NM_001243804.2:c.537A=	NP_001230733.1:p.Ile179=
NR_045044.2:n.934A=
NM_001178033.3:c.443A=	NP_001171504.1:p.Tyr148=