Canonical Allele Identifier: CA2579192512

Gene: ZFHX4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864250_76864252del , CM000670.2:g.76864250_76864252del	GRCh38
NC_000008.10:g.77776486_77776488del , CM000670.1:g.77776486_77776488del	GRCh37
NC_000008.9:g.77939041_77939043del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10536_10538del MANE Select	ENSP00000498627.1:p.Asn3513del
ENST00000518282.5:c.10458_10460del	ENSP00000430848.1:p.Asn3487del
ENST00000521891.6:c.10536_10538del	ENSP00000430497.2:p.Asn3513del
NM_024721.4:c.10536_10538del	NP_078997.4:p.Asn3513del
XM_011517592.1:c.10536_10538del	XP_011515894.1:p.Asn3513del
XM_011517593.1:c.10536_10538del	XP_011515895.1:p.Asn3513del
XM_011517594.1:c.10536_10538del	XP_011515896.1:p.Asn3513del
XM_011517595.1:c.10536_10538del	XP_011515897.1:p.Asn3513del
XM_011517596.1:c.10458_10460del	XP_011515898.1:p.Asn3487del
XM_011517597.1:c.10419_10421del	XP_011515899.1:p.Asn3474del
XM_011517592.3:c.10536_10538del	XP_011515894.1:p.Asn3513del
XM_011517593.2:c.10536_10538del	XP_011515895.1:p.Asn3513del
XM_011517594.2:c.10536_10538del	XP_011515896.1:p.Asn3513del
XM_011517595.2:c.10536_10538del	XP_011515897.1:p.Asn3513del
XM_011517596.2:c.10458_10460del	XP_011515898.1:p.Asn3487del
XM_011517597.2:c.10419_10421del	XP_011515899.1:p.Asn3474del
XM_017013845.1:c.10341_10343del	XP_016869334.1:p.Asn3448del
NM_024721.5:c.10536_10538del MANE Select	NP_078997.4:p.Asn3513del