Canonical Allele Identifier: CA413412275

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64141777T>C (hg19) ; chrX:g.64921897T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921897T>C , CM000685.2:g.64921897T>C	GRCh38
NC_000023.10:g.64141777T>C , CM000685.1:g.64141777T>C	GRCh37
NC_000023.9:g.64058502T>C	NCBI36
NG_021200.1:g.59637A>G
NG_021200.2:g.117848A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.76A>G	ENSP00000515193.1:p.Lys26Glu
ENST00000492653.6:c.145A>G	ENSP00000515192.1:p.Lys49Glu
ENST00000703133.1:c.*719A>G	ENSP00000515188.1:n.*719A>G
ENST00000703136.1:c.*103A>G	ENSP00000515190.1:n.*103A>G
ENST00000374839.8:c.145A>G MANE Select	ENSP00000363972.3:p.Lys49Glu
ENST00000337990.2:c.76A>G	ENSP00000338650.2:p.Lys26Glu
ENST00000374839.7:c.145A>G	ENSP00000363972.3:p.Lys49Glu
ENST00000447788.6:c.145A>G	ENSP00000399126.2:p.Lys49Glu
ENST00000476032.1:n.386A>G
ENST00000488608.5:n.301A>G
ENST00000488831.5:n.133A>G
ENST00000492653.5:n.241A>G
NM_001178032.2:c.76A>G	NP_001171503.1:p.Lys26Glu
NM_001178033.2:c.145A>G	NP_001171504.1:p.Lys49Glu
NM_001243804.1:c.76A>G	NP_001230733.1:p.Lys26Glu
NM_018684.3:c.145A>G	NP_061154.1:p.Lys49Glu
NR_045044.1:n.556A>G
NM_018684.4:c.145A>G MANE Select	NP_061154.1:p.Lys49Glu
NM_001178032.3:c.76A>G	NP_001171503.1:p.Lys26Glu
NM_001243804.2:c.76A>G	NP_001230733.1:p.Lys26Glu
NR_045044.2:n.473A>G
NM_001178033.3:c.145A>G	NP_001171504.1:p.Lys49Glu