Canonical Allele Identifier: CA413411164

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137730C>T (hg19) ; chrX:g.64917850C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917850C>T , CM000685.2:g.64917850C>T	GRCh38
NC_000023.10:g.64137730C>T , CM000685.1:g.64137730C>T	GRCh37
NC_000023.9:g.64054455C>T	NCBI36
NG_021200.1:g.63684G>A
NG_021200.2:g.121895G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*232G>A	ENSP00000515192.1:n.*232G>A
ENST00000703133.1:c.*1182G>A	ENSP00000515188.1:n.*1182G>A
ENST00000703136.1:c.*566G>A	ENSP00000515190.1:n.*566G>A
ENST00000374839.8:c.608G>A MANE Select	ENSP00000363972.3:p.Cys203Tyr
ENST00000337990.2:c.539G>A	ENSP00000338650.2:p.Cys180Tyr
ENST00000374839.7:c.608G>A	ENSP00000363972.3:p.Cys203Tyr
ENST00000447788.6:c.445G>A	ENSP00000399126.2:p.Ala149Thr
ENST00000488406.1:n.128G>A
ENST00000488608.5:n.2785G>A
ENST00000488831.5:n.596G>A
ENST00000492653.5:n.736G>A
NM_001178032.2:c.539G>A	NP_001171503.1:p.Cys180Tyr
NM_001178033.2:c.445G>A	NP_001171504.1:p.Ala149Thr
NM_001243804.1:c.539G>A	NP_001230733.1:p.Cys180Tyr
NM_018684.3:c.608G>A	NP_061154.1:p.Cys203Tyr
NR_045044.1:n.1019G>A
NM_018684.4:c.608G>A MANE Select	NP_061154.1:p.Cys203Tyr
NM_001178032.3:c.539G>A	NP_001171503.1:p.Cys180Tyr
NM_001243804.2:c.539G>A	NP_001230733.1:p.Cys180Tyr
NR_045044.2:n.936G>A
NM_001178033.3:c.445G>A	NP_001171504.1:p.Ala149Thr