Canonical Allele Identifier: CA413411157

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137727G>T (hg19) ; chrX:g.64917847G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917847G>T , CM000685.2:g.64917847G>T	GRCh38
NC_000023.10:g.64137727G>T , CM000685.1:g.64137727G>T	GRCh37
NC_000023.9:g.64054452G>T	NCBI36
NG_021200.1:g.63687C>A
NG_021200.2:g.121898C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*235C>A	ENSP00000515192.1:n.*235C>A
ENST00000703133.1:c.*1185C>A	ENSP00000515188.1:n.*1185C>A
ENST00000703136.1:c.*569C>A	ENSP00000515190.1:n.*569C>A
ENST00000374839.8:c.611C>A MANE Select	ENSP00000363972.3:p.Pro204His
ENST00000337990.2:c.542C>A	ENSP00000338650.2:p.Pro181His
ENST00000374839.7:c.611C>A	ENSP00000363972.3:p.Pro204His
ENST00000447788.6:c.448C>A	ENSP00000399126.2:p.Leu150Ile
ENST00000488406.1:n.131C>A
ENST00000488608.5:n.2788C>A
ENST00000488831.5:n.599C>A
ENST00000492653.5:n.739C>A
NM_001178032.2:c.542C>A	NP_001171503.1:p.Pro181His
NM_001178033.2:c.448C>A	NP_001171504.1:p.Leu150Ile
NM_001243804.1:c.542C>A	NP_001230733.1:p.Pro181His
NM_018684.3:c.611C>A	NP_061154.1:p.Pro204His
NR_045044.1:n.1022C>A
NM_018684.4:c.611C>A MANE Select	NP_061154.1:p.Pro204His
NM_001178032.3:c.542C>A	NP_001171503.1:p.Pro181His
NM_001243804.2:c.542C>A	NP_001230733.1:p.Pro181His
NR_045044.2:n.939C>A
NM_001178033.3:c.448C>A	NP_001171504.1:p.Leu150Ile