Canonical Allele Identifier: CA2340217196

Gene: NTF4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061306G= , CM000681.2:g.49061306G=	GRCh38
NC_000019.9:g.49564563G= , CM000681.1:g.49564563G=	GRCh37
NC_000019.8:g.54256375G=	NCBI36
NG_016289.1:g.7562C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000593537.2:c.*59C= MANE Select	ENSP00000469455.1:n.*59C=
ENST00000594938.2:c.*59C=	ENSP00000512387.1:n.*59C=
ENST00000595857.6:c.*59C=	ENSP00000471508.2:n.*59C=
ENST00000696088.1:c.*59C=	ENSP00000512384.1:n.*59C=
ENST00000696089.1:c.*59C=	ENSP00000512385.1:n.*59C=
ENST00000696090.1:c.*59C=	ENSP00000512386.1:n.*59C=
ENST00000696091.1:c.*59C=	ENSP00000512388.1:n.*59C=
ENST00000593537.1:c.692C=	ENSP00000469455.1:n.692C=
ENST00000599795.5:c.243+449C=	ENSP00000470689.1:n.243+449C=
NM_006179.4:c.*59C=	NP_006170.1:n.*59C=
XM_005258962.2:c.*59C=	XP_005259019.1:n.*59C=
XM_006723232.2:c.*59C=	XP_006723295.1:n.*59C=
XM_011527008.1:c.*59C=	XP_011525310.1:n.*59C=
XM_011527009.1:c.*59C=	XP_011525311.1:n.*59C=
XM_011527010.1:c.*59C=	XP_011525312.1:n.*59C=
XM_005258962.3:c.*59C=	XP_005259019.1:n.*59C=
XM_006723232.3:c.*59C=	XP_006723295.1:n.*59C=
XM_011527008.2:c.*59C=	XP_011525310.1:n.*59C=
XM_011527009.2:c.*59C=	XP_011525311.1:n.*59C=
XM_011527010.2:c.*59C=	XP_011525312.1:n.*59C=
XR_001753693.1:n.737C=
XR_001753694.1:n.737C=
NM_001395489.1:c.*59C=	NP_001382418.1:n.*59C=
NM_006179.5:c.*59C= MANE Select	NP_006170.1:n.*59C=