Canonical Allele Identifier: CA10433354

Gene: ZC4H2

Linked Data

• dbSNP Id: rs370023519
• ExAC: X:64137632 A / T
• gnomAD v2: X-64137632-A-T
• gnomAD v3: X-64917752-A-T
• gnomAD v4: X-64917752-A-T
• MyVariant Identifiers: chrX:g.64137632A>T (hg19) ; chrX:g.64917752A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917752A>T , CM000685.2:g.64917752A>T	GRCh38
NC_000023.10:g.64137632A>T , CM000685.1:g.64137632A>T	GRCh37
NC_000023.9:g.64054357A>T	NCBI36
NG_021200.1:g.63782T>A
NG_021200.2:g.121993T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703133.1:c.*1280T>A	ENSP00000515188.1:n.*1280T>A
ENST00000703136.1:c.*664T>A	ENSP00000515190.1:n.*664T>A
ENST00000374839.8:c.*31T>A MANE Select	ENSP00000363972.3:n.*31T>A
ENST00000337990.2:c.*31T>A	ENSP00000338650.2:n.*31T>A
ENST00000374839.7:c.*31T>A	ENSP00000363972.3:n.*31T>A
ENST00000447788.6:c.*12T>A	ENSP00000399126.2:n.*12T>A
ENST00000488406.1:n.226T>A
ENST00000488608.5:n.2883T>A
NM_001178032.2:c.*31T>A	NP_001171503.1:n.*31T>A
NM_001178033.2:c.*12T>A	NP_001171504.1:n.*12T>A
NM_001243804.1:c.*31T>A	NP_001230733.1:n.*31T>A
NM_018684.3:c.*31T>A	NP_061154.1:n.*31T>A
NR_045044.1:n.1117T>A
NM_018684.4:c.*31T>A MANE Select	NP_061154.1:n.*31T>A
NM_001178032.3:c.*31T>A	NP_001171503.1:n.*31T>A
NM_001243804.2:c.*31T>A	NP_001230733.1:n.*31T>A
NR_045044.2:n.1034T>A
NM_001178033.3:c.*12T>A	NP_001171504.1:n.*12T>A