Canonical Allele Identifier: CA10433370

Gene: ZC4H2

Linked Data

• dbSNP Id: rs779577578
• ExAC: X:64137786 G / T
• gnomAD v2: X-64137786-G-T
• gnomAD v3: X-64917906-G-T
• gnomAD v4: X-64917906-G-T
• MyVariant Identifiers: chrX:g.64137786G>T (hg19) ; chrX:g.64917906G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917906G>T , CM000685.2:g.64917906G>T	GRCh38
NC_000023.10:g.64137786G>T , CM000685.1:g.64137786G>T	GRCh37
NC_000023.9:g.64054511G>T	NCBI36
NG_021200.1:g.63628C>A
NG_021200.2:g.121839C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.493-10C>A	ENSP00000515193.1:n.493-10C>A
ENST00000492653.6:c.*186-10C>A	ENSP00000515192.1:n.*186-10C>A
ENST00000703133.1:c.*1136-10C>A	ENSP00000515188.1:n.*1136-10C>A
ENST00000703136.1:c.*520-10C>A	ENSP00000515190.1:n.*520-10C>A
ENST00000374839.8:c.562-10C>A MANE Select	ENSP00000363972.3:n.562-10C>A
ENST00000337990.2:c.493-10C>A	ENSP00000338650.2:n.493-10C>A
ENST00000374839.7:c.562-10C>A	ENSP00000363972.3:n.562-10C>A
ENST00000447788.6:c.399-10C>A	ENSP00000399126.2:n.399-10C>A
ENST00000476032.1:n.803-10C>A
ENST00000488406.1:n.82-10C>A
ENST00000488608.5:n.2729C>A
ENST00000488831.5:n.550-10C>A
ENST00000492653.5:n.690-10C>A
NM_001178032.2:c.493-10C>A	NP_001171503.1:n.493-10C>A
NM_001178033.2:c.399-10C>A	NP_001171504.1:n.399-10C>A
NM_001243804.1:c.493-10C>A	NP_001230733.1:n.493-10C>A
NM_018684.3:c.562-10C>A	NP_061154.1:n.562-10C>A
NR_045044.1:n.973-10C>A
NM_018684.4:c.562-10C>A MANE Select	NP_061154.1:n.562-10C>A
NM_001178032.3:c.493-10C>A	NP_001171503.1:n.493-10C>A
NM_001243804.2:c.493-10C>A	NP_001230733.1:n.493-10C>A
NR_045044.2:n.890-10C>A
NM_001178033.3:c.399-10C>A	NP_001171504.1:n.399-10C>A