Canonical Allele Identifier: CA2821519675

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921782A>G , CM000685.2:g.64921782A>G	GRCh38
NC_000023.10:g.64141662A>G , CM000685.1:g.64141662A>G	GRCh37
NC_000023.9:g.64058387A>G	NCBI36
NG_021200.1:g.59752T>C
NG_021200.2:g.117963T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.156+35T>C	ENSP00000515193.1:n.156+35T>C
ENST00000492653.6:c.225+35T>C	ENSP00000515192.1:n.225+35T>C
ENST00000703133.1:c.*799+35T>C	ENSP00000515188.1:n.*799+35T>C
ENST00000703136.1:c.*183+35T>C	ENSP00000515190.1:n.*183+35T>C
ENST00000374839.8:c.225+35T>C MANE Select	ENSP00000363972.3:n.225+35T>C
ENST00000337990.2:c.156+35T>C	ENSP00000338650.2:n.156+35T>C
ENST00000374839.7:c.225+35T>C	ENSP00000363972.3:n.225+35T>C
ENST00000447788.6:c.225+35T>C	ENSP00000399126.2:n.225+35T>C
ENST00000476032.1:n.466+35T>C
ENST00000488608.5:n.381+35T>C
ENST00000488831.5:n.213+35T>C
ENST00000492653.5:n.321+35T>C
NM_001178032.2:c.156+35T>C	NP_001171503.1:n.156+35T>C
NM_001178033.2:c.225+35T>C	NP_001171504.1:n.225+35T>C
NM_001243804.1:c.156+35T>C	NP_001230733.1:n.156+35T>C
NM_018684.3:c.225+35T>C	NP_061154.1:n.225+35T>C
NR_045044.1:n.636+35T>C
NM_018684.4:c.225+35T>C MANE Select	NP_061154.1:n.225+35T>C
NM_001178032.3:c.156+35T>C	NP_001171503.1:n.156+35T>C
NM_001243804.2:c.156+35T>C	NP_001230733.1:n.156+35T>C
NR_045044.2:n.553+35T>C
NM_001178033.3:c.225+35T>C	NP_001171504.1:n.225+35T>C