Canonical Allele Identifier: CA413411283

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64137771G>T (hg19) ; chrX:g.64917891G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64917891G>T , CM000685.2:g.64917891G>T	GRCh38
NC_000023.10:g.64137771G>T , CM000685.1:g.64137771G>T	GRCh37
NC_000023.9:g.64054496G>T	NCBI36
NG_021200.1:g.63643C>A
NG_021200.2:g.121854C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.498C>A	ENSP00000515193.1:p.Cys166Ter
ENST00000492653.6:c.*191C>A	ENSP00000515192.1:n.*191C>A
ENST00000703133.1:c.*1141C>A	ENSP00000515188.1:n.*1141C>A
ENST00000703136.1:c.*525C>A	ENSP00000515190.1:n.*525C>A
ENST00000374839.8:c.567C>A MANE Select	ENSP00000363972.3:p.Cys189Ter
ENST00000337990.2:c.498C>A	ENSP00000338650.2:p.Cys166Ter
ENST00000374839.7:c.567C>A	ENSP00000363972.3:p.Cys189Ter
ENST00000447788.6:c.404C>A	ENSP00000399126.2:p.Ala135Asp
ENST00000476032.1:n.808C>A
ENST00000488406.1:n.87C>A
ENST00000488608.5:n.2744C>A
ENST00000488831.5:n.555C>A
ENST00000492653.5:n.695C>A
NM_001178032.2:c.498C>A	NP_001171503.1:p.Cys166Ter
NM_001178033.2:c.404C>A	NP_001171504.1:p.Ala135Asp
NM_001243804.1:c.498C>A	NP_001230733.1:p.Cys166Ter
NM_018684.3:c.567C>A	NP_061154.1:p.Cys189Ter
NR_045044.1:n.978C>A
NM_018684.4:c.567C>A MANE Select	NP_061154.1:p.Cys189Ter
NM_001178032.3:c.498C>A	NP_001171503.1:p.Cys166Ter
NM_001243804.2:c.498C>A	NP_001230733.1:p.Cys166Ter
NR_045044.2:n.895C>A
NM_001178033.3:c.404C>A	NP_001171504.1:p.Ala135Asp