Canonical Allele Identifier: CA2693921943

Gene: ZC4H2

Linked Data

• gnomAD v4: X-64921805-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64921805G>A , CM000685.2:g.64921805G>A	GRCh38
NC_000023.10:g.64141685G>A , CM000685.1:g.64141685G>A	GRCh37
NC_000023.9:g.64058410G>A	NCBI36
NG_021200.1:g.59729C>T
NG_021200.2:g.117940C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476032.2:c.156+12C>T	ENSP00000515193.1:n.156+12C>T
ENST00000492653.6:c.225+12C>T	ENSP00000515192.1:n.225+12C>T
ENST00000703133.1:c.*799+12C>T	ENSP00000515188.1:n.*799+12C>T
ENST00000703136.1:c.*183+12C>T	ENSP00000515190.1:n.*183+12C>T
ENST00000374839.8:c.225+12C>T MANE Select	ENSP00000363972.3:n.225+12C>T
ENST00000337990.2:c.156+12C>T	ENSP00000338650.2:n.156+12C>T
ENST00000374839.7:c.225+12C>T	ENSP00000363972.3:n.225+12C>T
ENST00000447788.6:c.225+12C>T	ENSP00000399126.2:n.225+12C>T
ENST00000476032.1:n.466+12C>T
ENST00000488608.5:n.381+12C>T
ENST00000488831.5:n.213+12C>T
ENST00000492653.5:n.321+12C>T
NM_001178032.2:c.156+12C>T	NP_001171503.1:n.156+12C>T
NM_001178033.2:c.225+12C>T	NP_001171504.1:n.225+12C>T
NM_001243804.1:c.156+12C>T	NP_001230733.1:n.156+12C>T
NM_018684.3:c.225+12C>T	NP_061154.1:n.225+12C>T
NR_045044.1:n.636+12C>T
NM_018684.4:c.225+12C>T MANE Select	NP_061154.1:n.225+12C>T
NM_001178032.3:c.156+12C>T	NP_001171503.1:n.156+12C>T
NM_001243804.2:c.156+12C>T	NP_001230733.1:n.156+12C>T
NR_045044.2:n.553+12C>T
NM_001178033.3:c.225+12C>T	NP_001171504.1:n.225+12C>T