Canonical Allele Identifier: CA413411140

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137721C>T (hg19) ; chrX:g.64917841C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917841C>T , CM000685.2:g.64917841C>T	GRCh38
NC_000023.10:g.64137721C>T , CM000685.1:g.64137721C>T	GRCh37
NC_000023.9:g.64054446C>T	NCBI36
NG_021200.1:g.63693G>A
NG_021200.2:g.121904G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*241G>A	ENSP00000515192.1:n.*241G>A
ENST00000703133.1:c.*1191G>A	ENSP00000515188.1:n.*1191G>A
ENST00000703136.1:c.*575G>A	ENSP00000515190.1:n.*575G>A
ENST00000374839.8:c.617G>A MANE Select	ENSP00000363972.3:p.Cys206Tyr
ENST00000337990.2:c.548G>A	ENSP00000338650.2:p.Cys183Tyr
ENST00000374839.7:c.617G>A	ENSP00000363972.3:p.Cys206Tyr
ENST00000447788.6:c.454G>A	ENSP00000399126.2:p.Ala152Thr
ENST00000488406.1:n.137G>A
ENST00000488608.5:n.2794G>A
ENST00000488831.5:n.605G>A
ENST00000492653.5:n.745G>A
NM_001178032.2:c.548G>A	NP_001171503.1:p.Cys183Tyr
NM_001178033.2:c.454G>A	NP_001171504.1:p.Ala152Thr
NM_001243804.1:c.548G>A	NP_001230733.1:p.Cys183Tyr
NM_018684.3:c.617G>A	NP_061154.1:p.Cys206Tyr
NR_045044.1:n.1028G>A
NM_018684.4:c.617G>A MANE Select	NP_061154.1:p.Cys206Tyr
NM_001178032.3:c.548G>A	NP_001171503.1:p.Cys183Tyr
NM_001243804.2:c.548G>A	NP_001230733.1:p.Cys183Tyr
NR_045044.2:n.945G>A
NM_001178033.3:c.454G>A	NP_001171504.1:p.Ala152Thr