Canonical Allele Identifier: CA2433764002

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921823G= , CM000685.2:g.64921823G=	GRCh38
NC_000023.10:g.64141703G= , CM000685.1:g.64141703G=	GRCh37
NC_000023.9:g.64058428G=	NCBI36
NG_021200.1:g.59711C=
NG_021200.2:g.117922C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.150C=	ENSP00000515193.1:p.Ile50=
ENST00000492653.6:c.219C=	ENSP00000515192.1:p.Ile73=
ENST00000703133.1:c.*793C=	ENSP00000515188.1:n.*793C=
ENST00000703136.1:c.*177C=	ENSP00000515190.1:n.*177C=
ENST00000374839.8:c.219C= MANE Select	ENSP00000363972.3:p.Ile73=
ENST00000337990.2:c.150C=	ENSP00000338650.2:p.Ile50=
ENST00000374839.7:c.219C=	ENSP00000363972.3:p.Ile73=
ENST00000447788.6:c.219C=	ENSP00000399126.2:p.Ile73=
ENST00000476032.1:n.460C=
ENST00000488608.5:n.375C=
ENST00000488831.5:n.207C=
ENST00000492653.5:n.315C=
NM_001178032.2:c.150C=	NP_001171503.1:p.Ile50=
NM_001178033.2:c.219C=	NP_001171504.1:p.Ile73=
NM_001243804.1:c.150C=	NP_001230733.1:p.Ile50=
NM_018684.3:c.219C=	NP_061154.1:p.Ile73=
NR_045044.1:n.630C=
NM_018684.4:c.219C= MANE Select	NP_061154.1:p.Ile73=
NM_001178032.3:c.150C=	NP_001171503.1:p.Ile50=
NM_001243804.2:c.150C=	NP_001230733.1:p.Ile50=
NR_045044.2:n.547C=
NM_001178033.3:c.219C=	NP_001171504.1:p.Ile73=