Canonical Allele Identifier: CA855429011

Gene: ZFHX4

Linked Data

• dbSNP Id: rs1374716041
• gnomAD v4: 8-76864252-A-ACAC
• MyVariant Identifiers: chr8:g.77776488_77776489insCAC (hg19) ; chr8:g.76864252_76864253insCAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864254_76864256dup , CM000670.2:g.76864254_76864256dup	GRCh38
NC_000008.10:g.77776490_77776492dup , CM000670.1:g.77776490_77776492dup	GRCh37
NC_000008.9:g.77939045_77939047dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10540_10542dup MANE Select	ENSP00000498627.1:p.Thr3514_Tyr3515insThr
ENST00000518282.5:c.10462_10464dup	ENSP00000430848.1:p.Thr3488_Tyr3489insThr
ENST00000521891.6:c.10540_10542dup	ENSP00000430497.2:p.Thr3514_Tyr3515insThr
NM_024721.4:c.10540_10542dup	NP_078997.4:p.Thr3514_Tyr3515insThr
XM_011517592.1:c.10540_10542dup	XP_011515894.1:p.Thr3514_Tyr3515insThr
XM_011517593.1:c.10540_10542dup	XP_011515895.1:p.Thr3514_Tyr3515insThr
XM_011517594.1:c.10540_10542dup	XP_011515896.1:p.Thr3514_Tyr3515insThr
XM_011517595.1:c.10540_10542dup	XP_011515897.1:p.Thr3514_Tyr3515insThr
XM_011517596.1:c.10462_10464dup	XP_011515898.1:p.Thr3488_Tyr3489insThr
XM_011517597.1:c.10423_10425dup	XP_011515899.1:p.Thr3475_Tyr3476insThr
XM_011517592.3:c.10540_10542dup	XP_011515894.1:p.Thr3514_Tyr3515insThr
XM_011517593.2:c.10540_10542dup	XP_011515895.1:p.Thr3514_Tyr3515insThr
XM_011517594.2:c.10540_10542dup	XP_011515896.1:p.Thr3514_Tyr3515insThr
XM_011517595.2:c.10540_10542dup	XP_011515897.1:p.Thr3514_Tyr3515insThr
XM_011517596.2:c.10462_10464dup	XP_011515898.1:p.Thr3488_Tyr3489insThr
XM_011517597.2:c.10423_10425dup	XP_011515899.1:p.Thr3475_Tyr3476insThr
XM_017013845.1:c.10345_10347dup	XP_016869334.1:p.Thr3449_Tyr3450insThr
NM_024721.5:c.10540_10542dup MANE Select	NP_078997.4:p.Thr3514_Tyr3515insThr