Canonical Allele Identifier: CA2433764029

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921912G= , CM000685.2:g.64921912G=	GRCh38
NC_000023.10:g.64141792G= , CM000685.1:g.64141792G=	GRCh37
NC_000023.9:g.64058517G=	NCBI36
NG_021200.1:g.59622C=
NG_021200.2:g.117833C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.61C=	ENSP00000515193.1:p.His21=
ENST00000492653.6:c.130C=	ENSP00000515192.1:p.His44=
ENST00000703133.1:c.*704C=	ENSP00000515188.1:n.*704C=
ENST00000703136.1:c.*88C=	ENSP00000515190.1:n.*88C=
ENST00000374839.8:c.130C= MANE Select	ENSP00000363972.3:p.His44=
ENST00000337990.2:c.61C=	ENSP00000338650.2:p.His21=
ENST00000374839.7:c.130C=	ENSP00000363972.3:p.His44=
ENST00000447788.6:c.130C=	ENSP00000399126.2:p.His44=
ENST00000476032.1:n.371C=
ENST00000488608.5:n.286C=
ENST00000488831.5:n.118C=
ENST00000492653.5:n.226C=
NM_001178032.2:c.61C=	NP_001171503.1:p.His21=
NM_001178033.2:c.130C=	NP_001171504.1:p.His44=
NM_001243804.1:c.61C=	NP_001230733.1:p.His21=
NM_018684.3:c.130C=	NP_061154.1:p.His44=
NR_045044.1:n.541C=
NM_018684.4:c.130C= MANE Select	NP_061154.1:p.His44=
NM_001178032.3:c.61C=	NP_001171503.1:p.His21=
NM_001243804.2:c.61C=	NP_001230733.1:p.His21=
NR_045044.2:n.458C=
NM_001178033.3:c.130C=	NP_001171504.1:p.His44=