Canonical Allele Identifier: CA413411142

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137722A>G (hg19) ; chrX:g.64917842A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917842A>G , CM000685.2:g.64917842A>G	GRCh38
NC_000023.10:g.64137722A>G , CM000685.1:g.64137722A>G	GRCh37
NC_000023.9:g.64054447A>G	NCBI36
NG_021200.1:g.63692T>C
NG_021200.2:g.121903T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*240T>C	ENSP00000515192.1:n.*240T>C
ENST00000703133.1:c.*1190T>C	ENSP00000515188.1:n.*1190T>C
ENST00000703136.1:c.*574T>C	ENSP00000515190.1:n.*574T>C
ENST00000374839.8:c.616T>C MANE Select	ENSP00000363972.3:p.Cys206Arg
ENST00000337990.2:c.547T>C	ENSP00000338650.2:p.Cys183Arg
ENST00000374839.7:c.616T>C	ENSP00000363972.3:p.Cys206Arg
ENST00000447788.6:c.453T>C	ENSP00000399126.2:p.Phe151=
ENST00000488406.1:n.136T>C
ENST00000488608.5:n.2793T>C
ENST00000488831.5:n.604T>C
ENST00000492653.5:n.744T>C
NM_001178032.2:c.547T>C	NP_001171503.1:p.Cys183Arg
NM_001178033.2:c.453T>C	NP_001171504.1:p.Phe151=
NM_001243804.1:c.547T>C	NP_001230733.1:p.Cys183Arg
NM_018684.3:c.616T>C	NP_061154.1:p.Cys206Arg
NR_045044.1:n.1027T>C
NM_018684.4:c.616T>C MANE Select	NP_061154.1:p.Cys206Arg
NM_001178032.3:c.547T>C	NP_001171503.1:p.Cys183Arg
NM_001243804.2:c.547T>C	NP_001230733.1:p.Cys183Arg
NR_045044.2:n.944T>C
NM_001178033.3:c.453T>C	NP_001171504.1:p.Phe151=