Canonical Allele Identifier: CA2433764030

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921913C= , CM000685.2:g.64921913C=	GRCh38
NC_000023.10:g.64141793C= , CM000685.1:g.64141793C=	GRCh37
NC_000023.9:g.64058518C=	NCBI36
NG_021200.1:g.59621G=
NG_021200.2:g.117832G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.60G=	ENSP00000515193.1:p.Arg20=
ENST00000492653.6:c.129G=	ENSP00000515192.1:p.Arg43=
ENST00000703133.1:c.*703G=	ENSP00000515188.1:n.*703G=
ENST00000703136.1:c.*87G=	ENSP00000515190.1:n.*87G=
ENST00000374839.8:c.129G= MANE Select	ENSP00000363972.3:p.Arg43=
ENST00000337990.2:c.60G=	ENSP00000338650.2:p.Arg20=
ENST00000374839.7:c.129G=	ENSP00000363972.3:p.Arg43=
ENST00000447788.6:c.129G=	ENSP00000399126.2:p.Arg43=
ENST00000476032.1:n.370G=
ENST00000488608.5:n.285G=
ENST00000488831.5:n.117G=
ENST00000492653.5:n.225G=
NM_001178032.2:c.60G=	NP_001171503.1:p.Arg20=
NM_001178033.2:c.129G=	NP_001171504.1:p.Arg43=
NM_001243804.1:c.60G=	NP_001230733.1:p.Arg20=
NM_018684.3:c.129G=	NP_061154.1:p.Arg43=
NR_045044.1:n.540G=
NM_018684.4:c.129G= MANE Select	NP_061154.1:p.Arg43=
NM_001178032.3:c.60G=	NP_001171503.1:p.Arg20=
NM_001243804.2:c.60G=	NP_001230733.1:p.Arg20=
NR_045044.2:n.457G=
NM_001178033.3:c.129G=	NP_001171504.1:p.Arg43=