Canonical Allele Identifier: CA413412319

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64141795T>A (hg19) ; chrX:g.64921915T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921915T>A , CM000685.2:g.64921915T>A	GRCh38
NC_000023.10:g.64141795T>A , CM000685.1:g.64141795T>A	GRCh37
NC_000023.9:g.64058520T>A	NCBI36
NG_021200.1:g.59619A>T
NG_021200.2:g.117830A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.58A>T	ENSP00000515193.1:p.Arg20Trp
ENST00000492653.6:c.127A>T	ENSP00000515192.1:p.Arg43Trp
ENST00000703133.1:c.*701A>T	ENSP00000515188.1:n.*701A>T
ENST00000703136.1:c.*85A>T	ENSP00000515190.1:n.*85A>T
ENST00000374839.8:c.127A>T MANE Select	ENSP00000363972.3:p.Arg43Trp
ENST00000337990.2:c.58A>T	ENSP00000338650.2:p.Arg20Trp
ENST00000374839.7:c.127A>T	ENSP00000363972.3:p.Arg43Trp
ENST00000447788.6:c.127A>T	ENSP00000399126.2:p.Arg43Trp
ENST00000476032.1:n.368A>T
ENST00000488608.5:n.283A>T
ENST00000488831.5:n.115A>T
ENST00000492653.5:n.223A>T
NM_001178032.2:c.58A>T	NP_001171503.1:p.Arg20Trp
NM_001178033.2:c.127A>T	NP_001171504.1:p.Arg43Trp
NM_001243804.1:c.58A>T	NP_001230733.1:p.Arg20Trp
NM_018684.3:c.127A>T	NP_061154.1:p.Arg43Trp
NR_045044.1:n.538A>T
NM_018684.4:c.127A>T MANE Select	NP_061154.1:p.Arg43Trp
NM_001178032.3:c.58A>T	NP_001171503.1:p.Arg20Trp
NM_001243804.2:c.58A>T	NP_001230733.1:p.Arg20Trp
NR_045044.2:n.455A>T
NM_001178033.3:c.127A>T	NP_001171504.1:p.Arg43Trp