Canonical Allele Identifier: CA413411153

Gene: ZC4H2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*236T>C	ENSP00000515192.1:n.*236T>C
ENST00000703133.1:c.*1186T>C	ENSP00000515188.1:n.*1186T>C
ENST00000703136.1:c.*570T>C	ENSP00000515190.1:n.*570T>C
ENST00000374839.8:c.612T>C MANE Select	ENSP00000363972.3:p.Pro204=
ENST00000337990.2:c.543T>C	ENSP00000338650.2:p.Pro181=
ENST00000374839.7:c.612T>C	ENSP00000363972.3:p.Pro204=
ENST00000447788.6:c.449T>C	ENSP00000399126.2:p.Leu150Pro
ENST00000488406.1:n.132T>C
ENST00000488608.5:n.2789T>C
ENST00000488831.5:n.600T>C
ENST00000492653.5:n.740T>C
NM_001178032.2:c.543T>C	NP_001171503.1:p.Pro181=
NM_001178033.2:c.449T>C	NP_001171504.1:p.Leu150Pro
NM_001243804.1:c.543T>C	NP_001230733.1:p.Pro181=
NM_018684.3:c.612T>C	NP_061154.1:p.Pro204=
NR_045044.1:n.1023T>C
NM_018684.4:c.612T>C MANE Select	NP_061154.1:p.Pro204=
NM_001178032.3:c.543T>C	NP_001171503.1:p.Pro181=
NM_001243804.2:c.543T>C	NP_001230733.1:p.Pro181=
NR_045044.2:n.940T>C
NM_001178033.3:c.449T>C	NP_001171504.1:p.Leu150Pro