Canonical Allele Identifier: CA413411171

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137732T>G (hg19) ; chrX:g.64917852T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917852T>G , CM000685.2:g.64917852T>G	GRCh38
NC_000023.10:g.64137732T>G , CM000685.1:g.64137732T>G	GRCh37
NC_000023.9:g.64054457T>G	NCBI36
NG_021200.1:g.63682A>C
NG_021200.2:g.121893A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000492653.6:c.*230A>C	ENSP00000515192.1:n.*230A>C
ENST00000703133.1:c.*1180A>C	ENSP00000515188.1:n.*1180A>C
ENST00000703136.1:c.*564A>C	ENSP00000515190.1:n.*564A>C
ENST00000374839.8:c.606A>C MANE Select	ENSP00000363972.3:p.Ile202=
ENST00000337990.2:c.537A>C	ENSP00000338650.2:p.Ile179=
ENST00000374839.7:c.606A>C	ENSP00000363972.3:p.Ile202=
ENST00000447788.6:c.443A>C	ENSP00000399126.2:p.Tyr148Ser
ENST00000488406.1:n.126A>C
ENST00000488608.5:n.2783A>C
ENST00000488831.5:n.594A>C
ENST00000492653.5:n.734A>C
NM_001178032.2:c.537A>C	NP_001171503.1:p.Ile179=
NM_001178033.2:c.443A>C	NP_001171504.1:p.Tyr148Ser
NM_001243804.1:c.537A>C	NP_001230733.1:p.Ile179=
NM_018684.3:c.606A>C	NP_061154.1:p.Ile202=
NR_045044.1:n.1017A>C
NM_018684.4:c.606A>C MANE Select	NP_061154.1:p.Ile202=
NM_001178032.3:c.537A>C	NP_001171503.1:p.Ile179=
NM_001243804.2:c.537A>C	NP_001230733.1:p.Ile179=
NR_045044.2:n.934A>C
NM_001178033.3:c.443A>C	NP_001171504.1:p.Tyr148Ser