Canonical Allele Identifier: CA413411144

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137723A>C (hg19) ; chrX:g.64917843A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917843A>C , CM000685.2:g.64917843A>C	GRCh38
NC_000023.10:g.64137723A>C , CM000685.1:g.64137723A>C	GRCh37
NC_000023.9:g.64054448A>C	NCBI36
NG_021200.1:g.63691T>G
NG_021200.2:g.121902T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*239T>G	ENSP00000515192.1:n.*239T>G
ENST00000703133.1:c.*1189T>G	ENSP00000515188.1:n.*1189T>G
ENST00000703136.1:c.*573T>G	ENSP00000515190.1:n.*573T>G
ENST00000374839.8:c.615T>G MANE Select	ENSP00000363972.3:p.Leu205=
ENST00000337990.2:c.546T>G	ENSP00000338650.2:p.Leu182=
ENST00000374839.7:c.615T>G	ENSP00000363972.3:p.Leu205=
ENST00000447788.6:c.452T>G	ENSP00000399126.2:p.Phe151Cys
ENST00000488406.1:n.135T>G
ENST00000488608.5:n.2792T>G
ENST00000488831.5:n.603T>G
ENST00000492653.5:n.743T>G
NM_001178032.2:c.546T>G	NP_001171503.1:p.Leu182=
NM_001178033.2:c.452T>G	NP_001171504.1:p.Phe151Cys
NM_001243804.1:c.546T>G	NP_001230733.1:p.Leu182=
NM_018684.3:c.615T>G	NP_061154.1:p.Leu205=
NR_045044.1:n.1026T>G
NM_018684.4:c.615T>G MANE Select	NP_061154.1:p.Leu205=
NM_001178032.3:c.546T>G	NP_001171503.1:p.Leu182=
NM_001243804.2:c.546T>G	NP_001230733.1:p.Leu182=
NR_045044.2:n.943T>G
NM_001178033.3:c.452T>G	NP_001171504.1:p.Phe151Cys