Canonical Allele Identifier: CA2830545188

Gene: ZFHX4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864323_76864324insCTTCATG , CM000670.2:g.76864323_76864324insCTTCATG	GRCh38
NC_000008.10:g.77776559_77776560insCTTCATG , CM000670.1:g.77776559_77776560insCTTCATG	GRCh37
NC_000008.9:g.77939114_77939115insCTTCATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10609_10610insCTTCATG MANE Select	ENSP00000498627.1:p.Arg3537ThrfsTer?
ENST00000518282.5:c.10531_10532insCTTCATG	ENSP00000430848.1:p.Arg3511ThrfsTer?
ENST00000521891.6:c.10609_10610insCTTCATG	ENSP00000430497.2:p.Arg3537ThrfsTer?
NM_024721.4:c.10609_10610insCTTCATG	NP_078997.4:p.Arg3537ThrfsTer?
XM_011517592.1:c.10609_10610insCTTCATG	XP_011515894.1:p.Arg3537ThrfsTer?
XM_011517593.1:c.10609_10610insCTTCATG	XP_011515895.1:p.Arg3537ThrfsTer?
XM_011517594.1:c.10609_10610insCTTCATG	XP_011515896.1:p.Arg3537ThrfsTer?
XM_011517595.1:c.10609_10610insCTTCATG	XP_011515897.1:p.Arg3537ThrfsTer?
XM_011517596.1:c.10531_10532insCTTCATG	XP_011515898.1:p.Arg3511ThrfsTer?
XM_011517597.1:c.10492_10493insCTTCATG	XP_011515899.1:p.Arg3498ThrfsTer?
XM_011517592.3:c.10609_10610insCTTCATG	XP_011515894.1:p.Arg3537ThrfsTer?
XM_011517593.2:c.10609_10610insCTTCATG	XP_011515895.1:p.Arg3537ThrfsTer?
XM_011517594.2:c.10609_10610insCTTCATG	XP_011515896.1:p.Arg3537ThrfsTer?
XM_011517595.2:c.10609_10610insCTTCATG	XP_011515897.1:p.Arg3537ThrfsTer?
XM_011517596.2:c.10531_10532insCTTCATG	XP_011515898.1:p.Arg3511ThrfsTer?
XM_011517597.2:c.10492_10493insCTTCATG	XP_011515899.1:p.Arg3498ThrfsTer?
XM_017013845.1:c.10414_10415insCTTCATG	XP_016869334.1:p.Arg3472ThrfsTer?
NM_024721.5:c.10609_10610insCTTCATG MANE Select	NP_078997.4:p.Arg3537ThrfsTer?