Canonical Allele Identifier: CA413412376
Gene: ZC4H2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64921940C>G , CM000685.2:g.64921940C>G GRCh38
NC_000023.10:g.64141820C>G , CM000685.1:g.64141820C>G GRCh37
NC_000023.9:g.64058545C>G NCBI36
NG_021200.1:g.59594G>C
NG_021200.2:g.117805G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000476032.2:c.33G>C ENSP00000515193.1:p.Glu11Asp
ENST00000492653.6:c.102G>C ENSP00000515192.1:p.Glu34Asp
ENST00000703133.1:c.*676G>C ENSP00000515188.1:n.*676G>C
ENST00000703136.1:c.*60G>C ENSP00000515190.1:n.*60G>C
ENST00000374839.8:c.102G>C MANE Select ENSP00000363972.3:p.Glu34Asp
ENST00000337990.2:c.33G>C ENSP00000338650.2:p.Glu11Asp
ENST00000374839.7:c.102G>C ENSP00000363972.3:p.Glu34Asp
ENST00000447788.6:c.102G>C ENSP00000399126.2:p.Glu34Asp
ENST00000476032.1:n.343G>C
ENST00000488608.5:n.258G>C
ENST00000488831.5:n.90G>C
ENST00000492653.5:n.198G>C
NM_001178032.2:c.33G>C NP_001171503.1:p.Glu11Asp
NM_001178033.2:c.102G>C NP_001171504.1:p.Glu34Asp
NM_001243804.1:c.33G>C NP_001230733.1:p.Glu11Asp
NM_018684.3:c.102G>C NP_061154.1:p.Glu34Asp
NR_045044.1:n.513G>C
NM_018684.4:c.102G>C MANE Select NP_061154.1:p.Glu34Asp
NM_001178032.3:c.33G>C NP_001171503.1:p.Glu11Asp
NM_001243804.2:c.33G>C NP_001230733.1:p.Glu11Asp
NR_045044.2:n.430G>C
NM_001178033.3:c.102G>C NP_001171504.1:p.Glu34Asp