Canonical Allele Identifier: CA413412394

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64141827T>G (hg19) ; chrX:g.64921947T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921947T>G , CM000685.2:g.64921947T>G	GRCh38
NC_000023.10:g.64141827T>G , CM000685.1:g.64141827T>G	GRCh37
NC_000023.9:g.64058552T>G	NCBI36
NG_021200.1:g.59587A>C
NG_021200.2:g.117798A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.26A>C	ENSP00000515193.1:p.Lys9Thr
ENST00000492653.6:c.95A>C	ENSP00000515192.1:p.Lys32Thr
ENST00000703133.1:c.*669A>C	ENSP00000515188.1:n.*669A>C
ENST00000703136.1:c.*53A>C	ENSP00000515190.1:n.*53A>C
ENST00000374839.8:c.95A>C MANE Select	ENSP00000363972.3:p.Lys32Thr
ENST00000337990.2:c.26A>C	ENSP00000338650.2:p.Lys9Thr
ENST00000374839.7:c.95A>C	ENSP00000363972.3:p.Lys32Thr
ENST00000447788.6:c.95A>C	ENSP00000399126.2:p.Lys32Thr
ENST00000476032.1:n.336A>C
ENST00000488608.5:n.251A>C
ENST00000488831.5:n.83A>C
ENST00000492653.5:n.191A>C
NM_001178032.2:c.26A>C	NP_001171503.1:p.Lys9Thr
NM_001178033.2:c.95A>C	NP_001171504.1:p.Lys32Thr
NM_001243804.1:c.26A>C	NP_001230733.1:p.Lys9Thr
NM_018684.3:c.95A>C	NP_061154.1:p.Lys32Thr
NR_045044.1:n.506A>C
NM_018684.4:c.95A>C MANE Select	NP_061154.1:p.Lys32Thr
NM_001178032.3:c.26A>C	NP_001171503.1:p.Lys9Thr
NM_001243804.2:c.26A>C	NP_001230733.1:p.Lys9Thr
NR_045044.2:n.423A>C
NM_001178033.3:c.95A>C	NP_001171504.1:p.Lys32Thr