Canonical Allele Identifier: CA2123490998

Gene: ZFHX2 THTPA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23524204C= , CM000676.2:g.23524204C=	GRCh38
NC_000014.8:g.23993413C= , CM000676.1:g.23993413C=	GRCh37
NC_000014.7:g.23063253C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419474.5:c.5738G= (ZFHX2) MANE Select	ENSP00000413418.2:p.Arg1913=
ENST00000419474.4:c.5738G= (ZFHX2)	ENSP00000413418.2:p.Arg1913=
NM_033400.2:c.5738G= (ZFHX2)	NP_207646.2:p.Arg1913=
NR_046051.1:n.465+9788C= (THTPA)
NR_046052.1:n.245+9788C= (THTPA)
XM_005268135.2:c.2828G= (ZFHX2)	XP_005268192.1:p.Arg943=
XM_006720282.2:c.2588G= (ZFHX2)	XP_006720345.1:p.Arg863=
XM_011537244.1:c.5738G= (ZFHX2)	XP_011535546.1:p.Arg1913=
XM_011537245.1:c.5738G= (ZFHX2)	XP_011535547.1:p.Arg1913=
XM_011537246.1:c.5738G= (ZFHX2)	XP_011535548.1:p.Arg1913=
XM_011537247.1:c.5738G= (ZFHX2)	XP_011535549.1:p.Arg1913=
XM_011537248.1:c.5738G= (ZFHX2)	XP_011535550.1:p.Arg1913=
XM_011537249.1:c.5738G= (ZFHX2)	XP_011535551.1:p.Arg1913=
XM_011537250.1:c.5648G= (ZFHX2)	XP_011535552.1:p.Arg1883=
XM_011537251.1:c.5597G= (ZFHX2)	XP_011535553.1:p.Arg1866=
XM_011537252.1:c.2828G= (ZFHX2)	XP_011535554.1:p.Arg943=
XM_005268135.3:c.2828G= (ZFHX2)	XP_005268192.1:p.Arg943=
XM_011537245.3:c.5738G= (ZFHX2)	XP_011535547.1:p.Arg1913=
XM_011537246.3:c.5738G= (ZFHX2)	XP_011535548.1:p.Arg1913=
XM_011537247.2:c.5738G= (ZFHX2)	XP_011535549.1:p.Arg1913=
XM_011537252.2:c.2828G= (ZFHX2)	XP_011535554.1:p.Arg943=
XM_017021714.1:c.5738G= (ZFHX2)	XP_016877203.1:p.Arg1913=
XM_017021715.2:c.5660G= (ZFHX2)	XP_016877204.1:p.Arg1887=
XM_017021716.2:c.5750G= (ZFHX2)	XP_016877205.1:p.Arg1917=
XM_017021718.2:c.2588G= (ZFHX2)	XP_016877207.1:p.Arg863=
NM_033400.3:c.5738G= (ZFHX2) MANE Select	NP_207646.2:p.Arg1913=