Canonical Allele Identifier: CA645557356

Gene: ZFHX4

Linked Data

• COSMIC: COSM5943642 ; COSM5943643

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864205_76864209del , CM000670.2:g.76864205_76864209del	GRCh38
NC_000008.10:g.77776441_77776445del , CM000670.1:g.77776441_77776445del	GRCh37
NC_000008.9:g.77938996_77939000del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10491_10495del MANE Select	ENSP00000498627.1:p.Asn3498Ter
ENST00000518282.5:c.10413_10417del	ENSP00000430848.1:p.Asn3472Ter
ENST00000521891.6:c.10491_10495del	ENSP00000430497.2:p.Asn3498Ter
NM_024721.4:c.10491_10495del	NP_078997.4:p.Asn3498Ter
XM_011517592.1:c.10491_10495del	XP_011515894.1:p.Asn3498Ter
XM_011517593.1:c.10491_10495del	XP_011515895.1:p.Asn3498Ter
XM_011517594.1:c.10491_10495del	XP_011515896.1:p.Asn3498Ter
XM_011517595.1:c.10491_10495del	XP_011515897.1:p.Asn3498Ter
XM_011517596.1:c.10413_10417del	XP_011515898.1:p.Asn3472Ter
XM_011517597.1:c.10374_10378del	XP_011515899.1:p.Asn3459Ter
XM_011517592.3:c.10491_10495del	XP_011515894.1:p.Asn3498Ter
XM_011517593.2:c.10491_10495del	XP_011515895.1:p.Asn3498Ter
XM_011517594.2:c.10491_10495del	XP_011515896.1:p.Asn3498Ter
XM_011517595.2:c.10491_10495del	XP_011515897.1:p.Asn3498Ter
XM_011517596.2:c.10413_10417del	XP_011515898.1:p.Asn3472Ter
XM_011517597.2:c.10374_10378del	XP_011515899.1:p.Asn3459Ter
XM_017013845.1:c.10296_10300del	XP_016869334.1:p.Asn3433Ter
NM_024721.5:c.10491_10495del MANE Select	NP_078997.4:p.Asn3498Ter