Canonical Allele Identifier: CA413411597

Gene: ZC4H2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64919177C>T , CM000685.2:g.64919177C>T	GRCh38
NC_000023.10:g.64139057C>T , CM000685.1:g.64139057C>T	GRCh37
NC_000023.9:g.64055782C>T	NCBI36
NG_021200.1:g.62357G>A
NG_021200.2:g.120568G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_018684.4:c.426G>A MANE Select	NP_061154.1:p.Trp142Ter
ENST00000374839.8:c.426G>A MANE Select	ENSP00000363972.3:p.Trp142Ter
NM_001178032.2:c.357G>A	NP_001171503.1:p.Trp119Ter
NM_001178032.3:c.357G>A	NP_001171503.1:p.Trp119Ter
NM_001178033.2:c.398+904G>A	NP_001171504.1:n.398+904G>A
NM_001178033.3:c.398+904G>A	NP_001171504.1:n.398+904G>A
NM_001243804.1:c.357G>A	NP_001230733.1:p.Trp119Ter
NM_001243804.2:c.357G>A	NP_001230733.1:p.Trp119Ter
NM_018684.3:c.426G>A	NP_061154.1:p.Trp142Ter
NR_045044.1:n.837G>A
NR_045044.2:n.754G>A
ENST00000337990.2:c.357G>A	ENSP00000338650.2:p.Trp119Ter
ENST00000374839.7:c.426G>A	ENSP00000363972.3:p.Trp142Ter
ENST00000447788.6:c.398+904G>A	ENSP00000399126.2:n.398+904G>A
ENST00000476032.1:n.667G>A
ENST00000476032.2:c.357G>A	ENSP00000515193.1:p.Trp119Ter
ENST00000488406.1:n.59+16G>A
ENST00000488608.5:n.1458G>A
ENST00000488831.5:n.414G>A
ENST00000492653.5:n.554G>A
ENST00000492653.6:c.*50G>A	ENSP00000515192.1:n.*50G>A
ENST00000703133.1:c.*1000G>A	ENSP00000515188.1:n.*1000G>A
ENST00000703136.1:c.*384G>A	ENSP00000515190.1:n.*384G>A