Canonical Allele Identifier: CA461770865

Gene: ZFHX4

Linked Data

• MyVariant Identifiers: chr8:g.77776564T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76864328T>C , CM000670.2:g.76864328T>C	GRCh38
NC_000008.10:g.77776564T>C , CM000670.1:g.77776564T>C	GRCh37
NC_000008.9:g.77939119T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651372.2:c.10614T>C MANE Select	ENSP00000498627.1:p.Ala3538=
ENST00000518282.5:c.10536T>C	ENSP00000430848.1:p.Ala3512=
ENST00000521891.6:c.10614T>C	ENSP00000430497.2:p.Ala3538=
NM_024721.4:c.10614T>C	NP_078997.4:p.Ala3538=
XM_011517592.1:c.10614T>C	XP_011515894.1:p.Ala3538=
XM_011517593.1:c.10614T>C	XP_011515895.1:p.Ala3538=
XM_011517594.1:c.10614T>C	XP_011515896.1:p.Ala3538=
XM_011517595.1:c.10614T>C	XP_011515897.1:p.Ala3538=
XM_011517596.1:c.10536T>C	XP_011515898.1:p.Ala3512=
XM_011517597.1:c.10497T>C	XP_011515899.1:p.Ala3499=
XM_011517592.3:c.10614T>C	XP_011515894.1:p.Ala3538=
XM_011517593.2:c.10614T>C	XP_011515895.1:p.Ala3538=
XM_011517594.2:c.10614T>C	XP_011515896.1:p.Ala3538=
XM_011517595.2:c.10614T>C	XP_011515897.1:p.Ala3538=
XM_011517596.2:c.10536T>C	XP_011515898.1:p.Ala3512=
XM_011517597.2:c.10497T>C	XP_011515899.1:p.Ala3499=
XM_017013845.1:c.10419T>C	XP_016869334.1:p.Ala3473=
NM_024721.5:c.10614T>C MANE Select	NP_078997.4:p.Ala3538=