Canonical Allele Identifier: CA516907241

Gene: ZC4H2

Linked Data

• gnomAD v4: X-64921946-C-T
• COSMIC: COSM3914125 ; COSM3914126
• MyVariant Identifiers: chrX:g.64141826C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921946C>T , CM000685.2:g.64921946C>T	GRCh38
NC_000023.10:g.64141826C>T , CM000685.1:g.64141826C>T	GRCh37
NC_000023.9:g.64058551C>T	NCBI36
NG_021200.1:g.59588G>A
NG_021200.2:g.117799G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.27G>A	ENSP00000515193.1:p.Lys9=
ENST00000492653.6:c.96G>A	ENSP00000515192.1:p.Lys32=
ENST00000703133.1:c.*670G>A	ENSP00000515188.1:n.*670G>A
ENST00000703136.1:c.*54G>A	ENSP00000515190.1:n.*54G>A
ENST00000374839.8:c.96G>A MANE Select	ENSP00000363972.3:p.Lys32=
ENST00000337990.2:c.27G>A	ENSP00000338650.2:p.Lys9=
ENST00000374839.7:c.96G>A	ENSP00000363972.3:p.Lys32=
ENST00000447788.6:c.96G>A	ENSP00000399126.2:p.Lys32=
ENST00000476032.1:n.337G>A
ENST00000488608.5:n.252G>A
ENST00000488831.5:n.84G>A
ENST00000492653.5:n.192G>A
NM_001178032.2:c.27G>A	NP_001171503.1:p.Lys9=
NM_001178033.2:c.96G>A	NP_001171504.1:p.Lys32=
NM_001243804.1:c.27G>A	NP_001230733.1:p.Lys9=
NM_018684.3:c.96G>A	NP_061154.1:p.Lys32=
NR_045044.1:n.507G>A
NM_018684.4:c.96G>A MANE Select	NP_061154.1:p.Lys32=
NM_001178032.3:c.27G>A	NP_001171503.1:p.Lys9=
NM_001243804.2:c.27G>A	NP_001230733.1:p.Lys9=
NR_045044.2:n.424G>A
NM_001178033.3:c.96G>A	NP_001171504.1:p.Lys32=