Canonical Allele Identifier: CA2830545186

Gene: ZFHX4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864304_76864309del , CM000670.2:g.76864304_76864309del	GRCh38
NC_000008.10:g.77776540_77776545del , CM000670.1:g.77776540_77776545del	GRCh37
NC_000008.9:g.77939095_77939100del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10590_10595del MANE Select	ENSP00000498627.1:p.Phe3531_Gln3532del
ENST00000518282.5:c.10512_10517del	ENSP00000430848.1:p.Phe3505_Gln3506del
ENST00000521891.6:c.10590_10595del	ENSP00000430497.2:p.Phe3531_Gln3532del
NM_024721.4:c.10590_10595del	NP_078997.4:p.Phe3531_Gln3532del
XM_011517592.1:c.10590_10595del	XP_011515894.1:p.Phe3531_Gln3532del
XM_011517593.1:c.10590_10595del	XP_011515895.1:p.Phe3531_Gln3532del
XM_011517594.1:c.10590_10595del	XP_011515896.1:p.Phe3531_Gln3532del
XM_011517595.1:c.10590_10595del	XP_011515897.1:p.Phe3531_Gln3532del
XM_011517596.1:c.10512_10517del	XP_011515898.1:p.Phe3505_Gln3506del
XM_011517597.1:c.10473_10478del	XP_011515899.1:p.Phe3492_Gln3493del
XM_011517592.3:c.10590_10595del	XP_011515894.1:p.Phe3531_Gln3532del
XM_011517593.2:c.10590_10595del	XP_011515895.1:p.Phe3531_Gln3532del
XM_011517594.2:c.10590_10595del	XP_011515896.1:p.Phe3531_Gln3532del
XM_011517595.2:c.10590_10595del	XP_011515897.1:p.Phe3531_Gln3532del
XM_011517596.2:c.10512_10517del	XP_011515898.1:p.Phe3505_Gln3506del
XM_011517597.2:c.10473_10478del	XP_011515899.1:p.Phe3492_Gln3493del
XM_017013845.1:c.10395_10400del	XP_016869334.1:p.Phe3466_Gln3467del
NM_024721.5:c.10590_10595del MANE Select	NP_078997.4:p.Phe3531_Gln3532del