Canonical Allele Identifier: CA2814676586

Gene: NTF4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061333_49061334del , CM000681.2:g.49061333_49061334del	GRCh38
NC_000019.9:g.49564590_49564591del , CM000681.1:g.49564590_49564591del	GRCh37
NC_000019.8:g.54256402_54256403del	NCBI36
NG_016289.1:g.7534_7535del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593537.2:c.*31_*32del MANE Select	ENSP00000469455.1:n.*31_*32del
ENST00000594938.2:c.*31_*32del	ENSP00000512387.1:n.*31_*32del
ENST00000595857.6:c.*31_*32del	ENSP00000471508.2:n.*31_*32del
ENST00000696088.1:c.*31_*32del	ENSP00000512384.1:n.*31_*32del
ENST00000696089.1:c.*31_*32del	ENSP00000512385.1:n.*31_*32del
ENST00000696090.1:c.*31_*32del	ENSP00000512386.1:n.*31_*32del
ENST00000696091.1:c.*31_*32del	ENSP00000512388.1:n.*31_*32del
ENST00000593537.1:c.664_665del	ENSP00000469455.1:n.664_665del
ENST00000599795.5:c.243+421_243+422del	ENSP00000470689.1:n.243+421_243+422del
NM_006179.4:c.*31_*32del	NP_006170.1:n.*31_*32del
XM_005258962.2:c.*31_*32del	XP_005259019.1:n.*31_*32del
XM_006723232.2:c.*31_*32del	XP_006723295.1:n.*31_*32del
XM_011527008.1:c.*31_*32del	XP_011525310.1:n.*31_*32del
XM_011527009.1:c.*31_*32del	XP_011525311.1:n.*31_*32del
XM_011527010.1:c.*31_*32del	XP_011525312.1:n.*31_*32del
XM_005258962.3:c.*31_*32del	XP_005259019.1:n.*31_*32del
XM_006723232.3:c.*31_*32del	XP_006723295.1:n.*31_*32del
XM_011527008.2:c.*31_*32del	XP_011525310.1:n.*31_*32del
XM_011527009.2:c.*31_*32del	XP_011525311.1:n.*31_*32del
XM_011527010.2:c.*31_*32del	XP_011525312.1:n.*31_*32del
XR_001753693.1:n.709_710del
XR_001753694.1:n.709_710del
NM_001395489.1:c.*31_*32del	NP_001382418.1:n.*31_*32del
NM_006179.5:c.*31_*32del MANE Select	NP_006170.1:n.*31_*32del