Canonical Allele Identifier: CA2340217483

Gene: NTF4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061858A= , CM000681.2:g.49061858A=	GRCh38
NC_000019.9:g.49565115A= , CM000681.1:g.49565115A=	GRCh37
NC_000019.8:g.54256927A=	NCBI36
NG_016289.1:g.7010T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593537.2:c.140T= MANE Select	ENSP00000469455.1:p.Val47=
ENST00000594938.2:c.140T=	ENSP00000512387.1:p.Val47=
ENST00000595857.6:c.140T=	ENSP00000471508.2:p.Val47=
ENST00000696088.1:c.140T=	ENSP00000512384.1:p.Val47=
ENST00000696089.1:c.140T=	ENSP00000512385.1:p.Val47=
ENST00000696090.1:c.140T=	ENSP00000512386.1:p.Val47=
ENST00000696091.1:c.140T=	ENSP00000512388.1:p.Val47=
ENST00000593537.1:c.140T=	ENSP00000469455.1:p.Val47=
ENST00000595857.5:c.140T=	ENSP00000471508.1:p.Val47=
ENST00000599795.5:c.140T=	ENSP00000470689.1:p.Val47=
NM_006179.4:c.140T=	NP_006170.1:p.Val47=
XM_005258962.2:c.140T=	XP_005259019.1:p.Val47=
XM_006723232.2:c.140T=	XP_006723295.1:p.Val47=
XM_011527008.1:c.170T=	XP_011525310.1:p.Val57=
XM_011527009.1:c.140T=	XP_011525311.1:p.Val47=
XM_011527010.1:c.140T=	XP_011525312.1:p.Val47=
XM_005258962.3:c.140T=	XP_005259019.1:p.Val47=
XM_006723232.3:c.140T=	XP_006723295.1:p.Val47=
XM_011527008.2:c.170T=	XP_011525310.1:p.Val57=
XM_011527009.2:c.140T=	XP_011525311.1:p.Val47=
XM_011527010.2:c.140T=	XP_011525312.1:p.Val47=
XR_001753693.1:n.185T=
XR_001753694.1:n.185T=
NM_001395489.1:c.140T=	NP_001382418.1:p.Val47=
NM_006179.5:c.140T= MANE Select	NP_006170.1:p.Val47=