Canonical Allele Identifier: CA2340217125

Gene: NTF4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061103T= , CM000681.2:g.49061103T=	GRCh38
NC_000019.9:g.49564360T= , CM000681.1:g.49564360T=	GRCh37
NC_000019.8:g.54256172T=	NCBI36
NG_016289.1:g.7765A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000594938.2:c.*262A=	ENSP00000512387.1:n.*262A=
ENST00000595857.6:c.*262A=	ENSP00000471508.2:n.*262A=
ENST00000696088.1:c.*262A=	ENSP00000512384.1:n.*262A=
ENST00000696089.1:c.*262A=	ENSP00000512385.1:n.*262A=
ENST00000696090.1:c.*262A=	ENSP00000512386.1:n.*262A=
ENST00000696091.1:c.*262A=	ENSP00000512388.1:n.*262A=
ENST00000593537.1:c.895A=	ENSP00000469455.1:n.895A=
ENST00000599795.5:c.243+652A=	ENSP00000470689.1:n.243+652A=
XM_005258962.2:c.*262A=	XP_005259019.1:n.*262A=
XM_006723232.2:c.*262A=	XP_006723295.1:n.*262A=
XM_011527008.1:c.*262A=	XP_011525310.1:n.*262A=
XM_011527009.1:c.*262A=	XP_011525311.1:n.*262A=
XM_011527010.1:c.*262A=	XP_011525312.1:n.*262A=
XM_005258962.3:c.*262A=	XP_005259019.1:n.*262A=
XM_006723232.3:c.*262A=	XP_006723295.1:n.*262A=
XM_011527008.2:c.*262A=	XP_011525310.1:n.*262A=
XM_011527009.2:c.*262A=	XP_011525311.1:n.*262A=
XM_011527010.2:c.*262A=	XP_011525312.1:n.*262A=
XR_001753693.1:n.879+61A=
XR_001753694.1:n.879+61A=