Canonical Allele Identifier: CA413412377

Gene: ZC4H2

Linked Data

• MyVariant Identifiers: chrX:g.64141820C>A (hg19) ; chrX:g.64921940C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921940C>A , CM000685.2:g.64921940C>A	GRCh38
NC_000023.10:g.64141820C>A , CM000685.1:g.64141820C>A	GRCh37
NC_000023.9:g.64058545C>A	NCBI36
NG_021200.1:g.59594G>T
NG_021200.2:g.117805G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.33G>T	ENSP00000515193.1:p.Glu11Asp
ENST00000492653.6:c.102G>T	ENSP00000515192.1:p.Glu34Asp
ENST00000703133.1:c.*676G>T	ENSP00000515188.1:n.*676G>T
ENST00000703136.1:c.*60G>T	ENSP00000515190.1:n.*60G>T
ENST00000374839.8:c.102G>T MANE Select	ENSP00000363972.3:p.Glu34Asp
ENST00000337990.2:c.33G>T	ENSP00000338650.2:p.Glu11Asp
ENST00000374839.7:c.102G>T	ENSP00000363972.3:p.Glu34Asp
ENST00000447788.6:c.102G>T	ENSP00000399126.2:p.Glu34Asp
ENST00000476032.1:n.343G>T
ENST00000488608.5:n.258G>T
ENST00000488831.5:n.90G>T
ENST00000492653.5:n.198G>T
NM_001178032.2:c.33G>T	NP_001171503.1:p.Glu11Asp
NM_001178033.2:c.102G>T	NP_001171504.1:p.Glu34Asp
NM_001243804.1:c.33G>T	NP_001230733.1:p.Glu11Asp
NM_018684.3:c.102G>T	NP_061154.1:p.Glu34Asp
NR_045044.1:n.513G>T
NM_018684.4:c.102G>T MANE Select	NP_061154.1:p.Glu34Asp
NM_001178032.3:c.33G>T	NP_001171503.1:p.Glu11Asp
NM_001243804.2:c.33G>T	NP_001230733.1:p.Glu11Asp
NR_045044.2:n.430G>T
NM_001178033.3:c.102G>T	NP_001171504.1:p.Glu34Asp