Canonical Allele Identifier: CA413411061

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137693G>C (hg19) ; chrX:g.64917813G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917813G>C , CM000685.2:g.64917813G>C	GRCh38
NC_000023.10:g.64137693G>C , CM000685.1:g.64137693G>C	GRCh37
NC_000023.9:g.64054418G>C	NCBI36
NG_021200.1:g.63721C>G
NG_021200.2:g.121932C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492653.6:c.*269C>G	ENSP00000515192.1:n.*269C>G
ENST00000703133.1:c.*1219C>G	ENSP00000515188.1:n.*1219C>G
ENST00000703136.1:c.*603C>G	ENSP00000515190.1:n.*603C>G
ENST00000374839.8:c.645C>G MANE Select	ENSP00000363972.3:p.Pro215=
ENST00000337990.2:c.576C>G	ENSP00000338650.2:p.Pro192=
ENST00000374839.7:c.645C>G	ENSP00000363972.3:p.Pro215=
ENST00000447788.6:c.482C>G	ENSP00000399126.2:p.Pro161Arg
ENST00000488406.1:n.165C>G
ENST00000488608.5:n.2822C>G
ENST00000492653.5:n.773C>G
NM_001178032.2:c.576C>G	NP_001171503.1:p.Pro192=
NM_001178033.2:c.482C>G	NP_001171504.1:p.Pro161Arg
NM_001243804.1:c.576C>G	NP_001230733.1:p.Pro192=
NM_018684.3:c.645C>G	NP_061154.1:p.Pro215=
NR_045044.1:n.1056C>G
NM_018684.4:c.645C>G MANE Select	NP_061154.1:p.Pro215=
NM_001178032.3:c.576C>G	NP_001171503.1:p.Pro192=
NM_001243804.2:c.576C>G	NP_001230733.1:p.Pro192=
NR_045044.2:n.973C>G
NM_001178033.3:c.482C>G	NP_001171504.1:p.Pro161Arg