Canonical Allele Identifier: CA2832012907

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917945G>C , CM000685.2:g.64917945G>C	GRCh38
NC_000023.10:g.64137825G>C , CM000685.1:g.64137825G>C	GRCh37
NC_000023.9:g.64054550G>C	NCBI36
NG_021200.1:g.63589C>G
NG_021200.2:g.121800C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.493-49C>G	ENSP00000515193.1:n.493-49C>G
ENST00000492653.6:c.*186-49C>G	ENSP00000515192.1:n.*186-49C>G
ENST00000703133.1:c.*1136-49C>G	ENSP00000515188.1:n.*1136-49C>G
ENST00000703136.1:c.*520-49C>G	ENSP00000515190.1:n.*520-49C>G
ENST00000374839.8:c.562-49C>G MANE Select	ENSP00000363972.3:n.562-49C>G
ENST00000337990.2:c.493-49C>G	ENSP00000338650.2:n.493-49C>G
ENST00000374839.7:c.562-49C>G	ENSP00000363972.3:n.562-49C>G
ENST00000447788.6:c.399-49C>G	ENSP00000399126.2:n.399-49C>G
ENST00000476032.1:n.803-49C>G
ENST00000488406.1:n.82-49C>G
ENST00000488608.5:n.2690C>G
ENST00000488831.5:n.550-49C>G
ENST00000492653.5:n.690-49C>G
NM_001178032.2:c.493-49C>G	NP_001171503.1:n.493-49C>G
NM_001178033.2:c.399-49C>G	NP_001171504.1:n.399-49C>G
NM_001243804.1:c.493-49C>G	NP_001230733.1:n.493-49C>G
NM_018684.3:c.562-49C>G	NP_061154.1:n.562-49C>G
NR_045044.1:n.973-49C>G
NM_018684.4:c.562-49C>G MANE Select	NP_061154.1:n.562-49C>G
NM_001178032.3:c.493-49C>G	NP_001171503.1:n.493-49C>G
NM_001243804.2:c.493-49C>G	NP_001230733.1:n.493-49C>G
NR_045044.2:n.890-49C>G
NM_001178033.3:c.399-49C>G	NP_001171504.1:n.399-49C>G