Canonical Allele Identifier: CA4788567

Gene: ZFHX4

Linked Data

• dbSNP Id: rs780690860
• ExAC: 8:77776565 G / A
• gnomAD v2: 8-77776565-G-A
• gnomAD v4: 8-76864329-G-A
• MyVariant Identifiers: chr8:g.77776565G>A (hg19) ; chr8:g.76864329G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864329G>A , CM000670.2:g.76864329G>A	GRCh38
NC_000008.10:g.77776565G>A , CM000670.1:g.77776565G>A	GRCh37
NC_000008.9:g.77939120G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10615G>A MANE Select	ENSP00000498627.1:p.Ala3539Thr
ENST00000518282.5:c.10537G>A	ENSP00000430848.1:p.Ala3513Thr
ENST00000521891.6:c.10615G>A	ENSP00000430497.2:p.Ala3539Thr
NM_024721.4:c.10615G>A	NP_078997.4:p.Ala3539Thr
XM_011517592.1:c.10615G>A	XP_011515894.1:p.Ala3539Thr
XM_011517593.1:c.10615G>A	XP_011515895.1:p.Ala3539Thr
XM_011517594.1:c.10615G>A	XP_011515896.1:p.Ala3539Thr
XM_011517595.1:c.10615G>A	XP_011515897.1:p.Ala3539Thr
XM_011517596.1:c.10537G>A	XP_011515898.1:p.Ala3513Thr
XM_011517597.1:c.10498G>A	XP_011515899.1:p.Ala3500Thr
XM_011517592.3:c.10615G>A	XP_011515894.1:p.Ala3539Thr
XM_011517593.2:c.10615G>A	XP_011515895.1:p.Ala3539Thr
XM_011517594.2:c.10615G>A	XP_011515896.1:p.Ala3539Thr
XM_011517595.2:c.10615G>A	XP_011515897.1:p.Ala3539Thr
XM_011517596.2:c.10537G>A	XP_011515898.1:p.Ala3513Thr
XM_011517597.2:c.10498G>A	XP_011515899.1:p.Ala3500Thr
XM_017013845.1:c.10420G>A	XP_016869334.1:p.Ala3474Thr
NM_024721.5:c.10615G>A MANE Select	NP_078997.4:p.Ala3539Thr