Canonical Allele Identifier: CA2340217386

Gene: NTF4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061679G= , CM000681.2:g.49061679G=	GRCh38
NC_000019.9:g.49564936G= , CM000681.1:g.49564936G=	GRCh37
NC_000019.8:g.54256748G=	NCBI36
NG_016289.1:g.7189C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593537.2:c.319C= MANE Select	ENSP00000469455.1:p.Arg107=
ENST00000594938.2:c.319C=	ENSP00000512387.1:p.Arg107=
ENST00000595857.6:c.319C=	ENSP00000471508.2:p.Arg107=
ENST00000696088.1:c.319C=	ENSP00000512384.1:p.Arg107=
ENST00000696089.1:c.319C=	ENSP00000512385.1:p.Arg107=
ENST00000696090.1:c.319C=	ENSP00000512386.1:p.Arg107=
ENST00000696091.1:c.319C=	ENSP00000512388.1:p.Arg107=
ENST00000593537.1:c.319C=	ENSP00000469455.1:p.Arg107=
ENST00000595857.5:c.319C=	ENSP00000471508.1:p.Arg107=
ENST00000599795.5:c.243+76C=	ENSP00000470689.1:n.243+76C=
NM_006179.4:c.319C=	NP_006170.1:p.Arg107=
XM_005258962.2:c.319C=	XP_005259019.1:p.Arg107=
XM_006723232.2:c.319C=	XP_006723295.1:p.Arg107=
XM_011527008.1:c.349C=	XP_011525310.1:p.Arg117=
XM_011527009.1:c.319C=	XP_011525311.1:p.Arg107=
XM_011527010.1:c.319C=	XP_011525312.1:p.Arg107=
XM_005258962.3:c.319C=	XP_005259019.1:p.Arg107=
XM_006723232.3:c.319C=	XP_006723295.1:p.Arg107=
XM_011527008.2:c.349C=	XP_011525310.1:p.Arg117=
XM_011527009.2:c.319C=	XP_011525311.1:p.Arg107=
XM_011527010.2:c.319C=	XP_011525312.1:p.Arg107=
XR_001753693.1:n.364C=
XR_001753694.1:n.364C=
NM_001395489.1:c.319C=	NP_001382418.1:p.Arg107=
NM_006179.5:c.319C= MANE Select	NP_006170.1:p.Arg107=