Canonical Allele Identifier: CA4788569

Gene: ZFHX4

Linked Data

• dbSNP Id: rs748117974
• ExAC: 8:77776574 CCTT / C
• gnomAD v2: 8-77776574-CCTT-C
• gnomAD v3: 8-76864338-CCTT-C
• gnomAD v4: 8-76864338-CCTT-C
• COSMIC: COSM6036700 ; COSM6036701
• MyVariant Identifiers: chr8:g.77776575_77776577del (hg19) ; chr8:g.76864340_76864342del (hg38) ; chr8:g.76864339_76864341del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864344_76864346del , CM000670.2:g.76864344_76864346del	GRCh38
NC_000008.10:g.77776580_77776582del , CM000670.1:g.77776580_77776582del	GRCh37
NC_000008.9:g.77939135_77939137del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10630_10632del MANE Select	ENSP00000498627.1:p.Ser3544del
ENST00000518282.5:c.10552_10554del	ENSP00000430848.1:p.Ser3518del
ENST00000521891.6:c.10630_10632del	ENSP00000430497.2:p.Ser3544del
NM_024721.4:c.10630_10632del	NP_078997.4:p.Ser3544del
XM_011517592.1:c.10630_10632del	XP_011515894.1:p.Ser3544del
XM_011517593.1:c.10630_10632del	XP_011515895.1:p.Ser3544del
XM_011517594.1:c.10630_10632del	XP_011515896.1:p.Ser3544del
XM_011517595.1:c.10630_10632del	XP_011515897.1:p.Ser3544del
XM_011517596.1:c.10552_10554del	XP_011515898.1:p.Ser3518del
XM_011517597.1:c.10513_10515del	XP_011515899.1:p.Ser3505del
XM_011517592.3:c.10630_10632del	XP_011515894.1:p.Ser3544del
XM_011517593.2:c.10630_10632del	XP_011515895.1:p.Ser3544del
XM_011517594.2:c.10630_10632del	XP_011515896.1:p.Ser3544del
XM_011517595.2:c.10630_10632del	XP_011515897.1:p.Ser3544del
XM_011517596.2:c.10552_10554del	XP_011515898.1:p.Ser3518del
XM_011517597.2:c.10513_10515del	XP_011515899.1:p.Ser3505del
XM_017013845.1:c.10435_10437del	XP_016869334.1:p.Ser3479del
NM_024721.5:c.10630_10632del MANE Select	NP_078997.4:p.Ser3544del