Canonical Allele Identifier: CA2838991977
Gene: ZC4H2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64917928dup , CM000685.2:g.64917928dup GRCh38
NC_000023.10:g.64137808dup , CM000685.1:g.64137808dup GRCh37
NC_000023.9:g.64054533dup NCBI36
NG_021200.1:g.63606dup
NG_021200.2:g.121817dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000476032.2:c.493-32dup ENSP00000515193.1:n.493-32dup
ENST00000492653.6:c.*186-32dup ENSP00000515192.1:n.*186-32dup
ENST00000703133.1:c.*1136-32dup ENSP00000515188.1:n.*1136-32dup
ENST00000703136.1:c.*520-32dup ENSP00000515190.1:n.*520-32dup
ENST00000374839.8:c.562-32dup MANE Select ENSP00000363972.3:n.562-32dup
ENST00000337990.2:c.493-32dup ENSP00000338650.2:n.493-32dup
ENST00000374839.7:c.562-32dup ENSP00000363972.3:n.562-32dup
ENST00000447788.6:c.399-32dup ENSP00000399126.2:n.399-32dup
ENST00000476032.1:n.803-32dup
ENST00000488406.1:n.82-32dup
ENST00000488608.5:n.2707dup
ENST00000488831.5:n.550-32dup
ENST00000492653.5:n.690-32dup
NM_001178032.2:c.493-32dup NP_001171503.1:n.493-32dup
NM_001178033.2:c.399-32dup NP_001171504.1:n.399-32dup
NM_001243804.1:c.493-32dup NP_001230733.1:n.493-32dup
NM_018684.3:c.562-32dup NP_061154.1:n.562-32dup
NR_045044.1:n.973-32dup
NM_018684.4:c.562-32dup MANE Select NP_061154.1:n.562-32dup
NM_001178032.3:c.493-32dup NP_001171503.1:n.493-32dup
NM_001243804.2:c.493-32dup NP_001230733.1:n.493-32dup
NR_045044.2:n.890-32dup
NM_001178033.3:c.399-32dup NP_001171504.1:n.399-32dup