Canonical Allele Identifier: CA2340217299

Gene: NTF4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061493C= , CM000681.2:g.49061493C=	GRCh38
NC_000019.9:g.49564750C= , CM000681.1:g.49564750C=	GRCh37
NC_000019.8:g.54256562C=	NCBI36
NG_016289.1:g.7375G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593537.2:c.505G= MANE Select	ENSP00000469455.1:p.Glu169=
ENST00000594938.2:c.505G=	ENSP00000512387.1:p.Glu169=
ENST00000595857.6:c.505G=	ENSP00000471508.2:p.Glu169=
ENST00000696088.1:c.505G=	ENSP00000512384.1:p.Glu169=
ENST00000696089.1:c.505G=	ENSP00000512385.1:p.Glu169=
ENST00000696090.1:c.505G=	ENSP00000512386.1:p.Glu169=
ENST00000696091.1:c.505G=	ENSP00000512388.1:p.Glu169=
ENST00000593537.1:c.505G=	ENSP00000469455.1:p.Glu169=
ENST00000599795.5:c.243+262G=	ENSP00000470689.1:n.243+262G=
NM_006179.4:c.505G=	NP_006170.1:p.Glu169=
XM_005258962.2:c.505G=	XP_005259019.1:p.Glu169=
XM_006723232.2:c.505G=	XP_006723295.1:p.Glu169=
XM_011527008.1:c.535G=	XP_011525310.1:p.Glu179=
XM_011527009.1:c.505G=	XP_011525311.1:p.Glu169=
XM_011527010.1:c.505G=	XP_011525312.1:p.Glu169=
XM_005258962.3:c.505G=	XP_005259019.1:p.Glu169=
XM_006723232.3:c.505G=	XP_006723295.1:p.Glu169=
XM_011527008.2:c.535G=	XP_011525310.1:p.Glu179=
XM_011527009.2:c.505G=	XP_011525311.1:p.Glu169=
XM_011527010.2:c.505G=	XP_011525312.1:p.Glu169=
XR_001753693.1:n.550G=
XR_001753694.1:n.550G=
NM_001395489.1:c.505G=	NP_001382418.1:p.Glu169=
NM_006179.5:c.505G= MANE Select	NP_006170.1:p.Glu169=