Canonical Allele Identifier: CA583367004

Gene: ZFHX4

Linked Data

• dbSNP Id: rs1253654532
• gnomAD v2: 8-77776624-GTGCAGCACC-G
• gnomAD v4: 8-76864388-GTGCAGCACC-G
• MyVariant Identifiers: chr8:g.77776625_77776633del (hg19) ; chr8:g.76864389_76864397del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864390_76864398del , CM000670.2:g.76864390_76864398del	GRCh38
NC_000008.10:g.77776626_77776634del , CM000670.1:g.77776626_77776634del	GRCh37
NC_000008.9:g.77939181_77939189del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10676_10684del MANE Select	ENSP00000498627.1:p.Cys3559_Thr3561del
ENST00000518282.5:c.10598_10606del	ENSP00000430848.1:p.Cys3533_Thr3535del
ENST00000521891.6:c.10676_10684del	ENSP00000430497.2:p.Cys3559_Thr3561del
NM_024721.4:c.10676_10684del	NP_078997.4:p.Cys3559_Thr3561del
XM_011517592.1:c.10676_10684del	XP_011515894.1:p.Cys3559_Thr3561del
XM_011517593.1:c.10676_10684del	XP_011515895.1:p.Cys3559_Thr3561del
XM_011517594.1:c.10676_10684del	XP_011515896.1:p.Cys3559_Thr3561del
XM_011517595.1:c.10676_10684del	XP_011515897.1:p.Cys3559_Thr3561del
XM_011517596.1:c.10598_10606del	XP_011515898.1:p.Cys3533_Thr3535del
XM_011517597.1:c.10559_10567del	XP_011515899.1:p.Cys3520_Thr3522del
XM_011517592.3:c.10676_10684del	XP_011515894.1:p.Cys3559_Thr3561del
XM_011517593.2:c.10676_10684del	XP_011515895.1:p.Cys3559_Thr3561del
XM_011517594.2:c.10676_10684del	XP_011515896.1:p.Cys3559_Thr3561del
XM_011517595.2:c.10676_10684del	XP_011515897.1:p.Cys3559_Thr3561del
XM_011517596.2:c.10598_10606del	XP_011515898.1:p.Cys3533_Thr3535del
XM_011517597.2:c.10559_10567del	XP_011515899.1:p.Cys3520_Thr3522del
XM_017013845.1:c.10481_10489del	XP_016869334.1:p.Cys3494_Thr3496del
NM_024721.5:c.10676_10684del MANE Select	NP_078997.4:p.Cys3559_Thr3561del