Canonical Allele Identifier: CA8163798

Gene: ZFHX3 ZFHX3-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.72798236T>A , CM000678.2:g.72798236T>A	GRCh38
NC_000016.9:g.72832135T>A , CM000678.1:g.72832135T>A	GRCh37
NC_000016.8:g.71389636T>A	NCBI36
NG_013211.1:g.265400A>T
NG_013211.2:g.1098696A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006885.4:c.4446A>T (ZFHX3) MANE Select	NP_008816.3:p.Ala1482=
ENST00000268489.10:c.4446A>T (ZFHX3) MANE Select	ENSP00000268489.5:p.Ala1482=
NM_001164766.1:c.1704A>T (ZFHX3)	NP_001158238.1:p.Ala568=
NM_001164766.2:c.1704A>T (ZFHX3)	NP_001158238.1:p.Ala568=
NM_001386735.1:c.4446A>T (ZFHX3)	NP_001373664.1:p.Ala1482=
NM_006885.3:c.4446A>T (ZFHX3)	NP_008816.3:p.Ala1482=
NR_171702.1:n.391-22537T>A (ZFHX3-AS1)
NR_171703.1:n.439+16417T>A (ZFHX3-AS1)
NR_171704.1:n.348-22537T>A (ZFHX3-AS1)
ENST00000268489.9:c.4446A>T (ZFHX3)	ENSP00000268489.5:p.Ala1482=
ENST00000397992.5:c.1704A>T (ZFHX3)	ENSP00000438926.3:p.Ala568=
ENST00000641206.2:c.4446A>T (ZFHX3)	ENSP00000493252.1:p.Ala1482=
XM_005255957.2:c.4443A>T (ZFHX3)	XP_005256014.1:p.Ala1481=
XM_005255957.4:c.4443A>T (ZFHX3)	XP_005256014.1:p.Ala1481=
XM_017023251.2:c.1797A>T (ZFHX3)	XP_016878740.1:p.Ala599=
XM_024450291.1:c.1794A>T (ZFHX3)	XP_024306059.1:p.Ala598=
XR_001752372.2:n.2152+5092T>A (ZFHX3-AS1)
XR_002957886.1:n.1998+5092T>A (ZFHX3-AS1)
XR_933723.1:n.194+5092T>A