Canonical Allele Identifier: CA413411152

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137726A>C (hg19) ; chrX:g.64917846A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917846A>C , CM000685.2:g.64917846A>C	GRCh38
NC_000023.10:g.64137726A>C , CM000685.1:g.64137726A>C	GRCh37
NC_000023.9:g.64054451A>C	NCBI36
NG_021200.1:g.63688T>G
NG_021200.2:g.121899T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*236T>G	ENSP00000515192.1:n.*236T>G
ENST00000703133.1:c.*1186T>G	ENSP00000515188.1:n.*1186T>G
ENST00000703136.1:c.*570T>G	ENSP00000515190.1:n.*570T>G
ENST00000374839.8:c.612T>G MANE Select	ENSP00000363972.3:p.Pro204=
ENST00000337990.2:c.543T>G	ENSP00000338650.2:p.Pro181=
ENST00000374839.7:c.612T>G	ENSP00000363972.3:p.Pro204=
ENST00000447788.6:c.449T>G	ENSP00000399126.2:p.Leu150Arg
ENST00000488406.1:n.132T>G
ENST00000488608.5:n.2789T>G
ENST00000488831.5:n.600T>G
ENST00000492653.5:n.740T>G
NM_001178032.2:c.543T>G	NP_001171503.1:p.Pro181=
NM_001178033.2:c.449T>G	NP_001171504.1:p.Leu150Arg
NM_001243804.1:c.543T>G	NP_001230733.1:p.Pro181=
NM_018684.3:c.612T>G	NP_061154.1:p.Pro204=
NR_045044.1:n.1023T>G
NM_018684.4:c.612T>G MANE Select	NP_061154.1:p.Pro204=
NM_001178032.3:c.543T>G	NP_001171503.1:p.Pro181=
NM_001243804.2:c.543T>G	NP_001230733.1:p.Pro181=
NR_045044.2:n.940T>G
NM_001178033.3:c.449T>G	NP_001171504.1:p.Leu150Arg