Canonical Allele Identifier: CA2830545183

Gene: ZFHX4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864295_76864296insTGG , CM000670.2:g.76864295_76864296insTGG	GRCh38
NC_000008.10:g.77776531_77776532insTGG , CM000670.1:g.77776531_77776532insTGG	GRCh37
NC_000008.9:g.77939086_77939087insTGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10581_10582insTGG MANE Select	ENSP00000498627.1:p.Pro3527_Asn3528insTrp
ENST00000518282.5:c.10503_10504insTGG	ENSP00000430848.1:p.Pro3501_Asn3502insTrp
ENST00000521891.6:c.10581_10582insTGG	ENSP00000430497.2:p.Pro3527_Asn3528insTrp
NM_024721.4:c.10581_10582insTGG	NP_078997.4:p.Pro3527_Asn3528insTrp
XM_011517592.1:c.10581_10582insTGG	XP_011515894.1:p.Pro3527_Asn3528insTrp
XM_011517593.1:c.10581_10582insTGG	XP_011515895.1:p.Pro3527_Asn3528insTrp
XM_011517594.1:c.10581_10582insTGG	XP_011515896.1:p.Pro3527_Asn3528insTrp
XM_011517595.1:c.10581_10582insTGG	XP_011515897.1:p.Pro3527_Asn3528insTrp
XM_011517596.1:c.10503_10504insTGG	XP_011515898.1:p.Pro3501_Asn3502insTrp
XM_011517597.1:c.10464_10465insTGG	XP_011515899.1:p.Pro3488_Asn3489insTrp
XM_011517592.3:c.10581_10582insTGG	XP_011515894.1:p.Pro3527_Asn3528insTrp
XM_011517593.2:c.10581_10582insTGG	XP_011515895.1:p.Pro3527_Asn3528insTrp
XM_011517594.2:c.10581_10582insTGG	XP_011515896.1:p.Pro3527_Asn3528insTrp
XM_011517595.2:c.10581_10582insTGG	XP_011515897.1:p.Pro3527_Asn3528insTrp
XM_011517596.2:c.10503_10504insTGG	XP_011515898.1:p.Pro3501_Asn3502insTrp
XM_011517597.2:c.10464_10465insTGG	XP_011515899.1:p.Pro3488_Asn3489insTrp
XM_017013845.1:c.10386_10387insTGG	XP_016869334.1:p.Pro3462_Asn3463insTrp
NM_024721.5:c.10581_10582insTGG MANE Select	NP_078997.4:p.Pro3527_Asn3528insTrp