Canonical Allele Identifier: CA2519240532

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921793_64921794del , CM000685.2:g.64921793_64921794del	GRCh38
NC_000023.10:g.64141673_64141674del , CM000685.1:g.64141673_64141674del	GRCh37
NC_000023.9:g.64058398_64058399del	NCBI36
NG_021200.1:g.59743_59744del
NG_021200.2:g.117954_117955del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.156+26_156+27del	ENSP00000515193.1:n.156+26_156+27del
ENST00000492653.6:c.225+26_225+27del	ENSP00000515192.1:n.225+26_225+27del
ENST00000703133.1:c.*799+26_*799+27del	ENSP00000515188.1:n.*799+26_*799+27del
ENST00000703136.1:c.*183+26_*183+27del	ENSP00000515190.1:n.*183+26_*183+27del
ENST00000374839.8:c.225+26_225+27del MANE Select	ENSP00000363972.3:n.225+26_225+27del
ENST00000337990.2:c.156+26_156+27del	ENSP00000338650.2:n.156+26_156+27del
ENST00000374839.7:c.225+26_225+27del	ENSP00000363972.3:n.225+26_225+27del
ENST00000447788.6:c.225+26_225+27del	ENSP00000399126.2:n.225+26_225+27del
ENST00000476032.1:n.466+26_466+27del
ENST00000488608.5:n.381+26_381+27del
ENST00000488831.5:n.213+26_213+27del
ENST00000492653.5:n.321+26_321+27del
NM_001178032.2:c.156+26_156+27del	NP_001171503.1:n.156+26_156+27del
NM_001178033.2:c.225+26_225+27del	NP_001171504.1:n.225+26_225+27del
NM_001243804.1:c.156+26_156+27del	NP_001230733.1:n.156+26_156+27del
NM_018684.3:c.225+26_225+27del	NP_061154.1:n.225+26_225+27del
NR_045044.1:n.636+26_636+27del
NM_018684.4:c.225+26_225+27del MANE Select	NP_061154.1:n.225+26_225+27del
NM_001178032.3:c.156+26_156+27del	NP_001171503.1:n.156+26_156+27del
NM_001243804.2:c.156+26_156+27del	NP_001230733.1:n.156+26_156+27del
NR_045044.2:n.553+26_553+27del
NM_001178033.3:c.225+26_225+27del	NP_001171504.1:n.225+26_225+27del