Canonical Allele Identifier: CA2433764006

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921831C= , CM000685.2:g.64921831C=	GRCh38
NC_000023.10:g.64141711C= , CM000685.1:g.64141711C=	GRCh37
NC_000023.9:g.64058436C=	NCBI36
NG_021200.1:g.59703G=
NG_021200.2:g.117914G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.142G=	ENSP00000515193.1:p.Ala48=
ENST00000492653.6:c.211G=	ENSP00000515192.1:p.Ala71=
ENST00000703133.1:c.*785G=	ENSP00000515188.1:n.*785G=
ENST00000703136.1:c.*169G=	ENSP00000515190.1:n.*169G=
ENST00000374839.8:c.211G= MANE Select	ENSP00000363972.3:p.Ala71=
ENST00000337990.2:c.142G=	ENSP00000338650.2:p.Ala48=
ENST00000374839.7:c.211G=	ENSP00000363972.3:p.Ala71=
ENST00000447788.6:c.211G=	ENSP00000399126.2:p.Ala71=
ENST00000476032.1:n.452G=
ENST00000488608.5:n.367G=
ENST00000488831.5:n.199G=
ENST00000492653.5:n.307G=
NM_001178032.2:c.142G=	NP_001171503.1:p.Ala48=
NM_001178033.2:c.211G=	NP_001171504.1:p.Ala71=
NM_001243804.1:c.142G=	NP_001230733.1:p.Ala48=
NM_018684.3:c.211G=	NP_061154.1:p.Ala71=
NR_045044.1:n.622G=
NM_018684.4:c.211G= MANE Select	NP_061154.1:p.Ala71=
NM_001178032.3:c.142G=	NP_001171503.1:p.Ala48=
NM_001243804.2:c.142G=	NP_001230733.1:p.Ala48=
NR_045044.2:n.539G=
NM_001178033.3:c.211G=	NP_001171504.1:p.Ala71=