Canonical Allele Identifier: CA413411174

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137733A>C (hg19) ; chrX:g.64917853A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917853A>C , CM000685.2:g.64917853A>C	GRCh38
NC_000023.10:g.64137733A>C , CM000685.1:g.64137733A>C	GRCh37
NC_000023.9:g.64054458A>C	NCBI36
NG_021200.1:g.63681T>G
NG_021200.2:g.121892T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*229T>G	ENSP00000515192.1:n.*229T>G
ENST00000703133.1:c.*1179T>G	ENSP00000515188.1:n.*1179T>G
ENST00000703136.1:c.*563T>G	ENSP00000515190.1:n.*563T>G
ENST00000374839.8:c.605T>G MANE Select	ENSP00000363972.3:p.Ile202Arg
ENST00000337990.2:c.536T>G	ENSP00000338650.2:p.Ile179Arg
ENST00000374839.7:c.605T>G	ENSP00000363972.3:p.Ile202Arg
ENST00000447788.6:c.442T>G	ENSP00000399126.2:p.Tyr148Asp
ENST00000488406.1:n.125T>G
ENST00000488608.5:n.2782T>G
ENST00000488831.5:n.593T>G
ENST00000492653.5:n.733T>G
NM_001178032.2:c.536T>G	NP_001171503.1:p.Ile179Arg
NM_001178033.2:c.442T>G	NP_001171504.1:p.Tyr148Asp
NM_001243804.1:c.536T>G	NP_001230733.1:p.Ile179Arg
NM_018684.3:c.605T>G	NP_061154.1:p.Ile202Arg
NR_045044.1:n.1016T>G
NM_018684.4:c.605T>G MANE Select	NP_061154.1:p.Ile202Arg
NM_001178032.3:c.536T>G	NP_001171503.1:p.Ile179Arg
NM_001243804.2:c.536T>G	NP_001230733.1:p.Ile179Arg
NR_045044.2:n.933T>G
NM_001178033.3:c.442T>G	NP_001171504.1:p.Tyr148Asp