Canonical Allele Identifier: CA2340217224

Gene: NTF4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061350_49061351delinsTC , CM000681.2:g.49061350_49061351delinsTC	GRCh38
NC_000019.9:g.49564607_49564608delinsTC , CM000681.1:g.49564607_49564608delinsTC	GRCh37
NC_000019.8:g.54256419_54256420delinsTC	NCBI36
NG_016289.1:g.7517_7518delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593537.2:c.*14_*15delinsGA MANE Select	ENSP00000469455.1:n.*14_*15delinsGA
ENST00000594938.2:c.*14_*15delinsGA	ENSP00000512387.1:n.*14_*15delinsGA
ENST00000595857.6:c.*14_*15delinsGA	ENSP00000471508.2:n.*14_*15delinsGA
ENST00000696088.1:c.*14_*15delinsGA	ENSP00000512384.1:n.*14_*15delinsGA
ENST00000696089.1:c.*14_*15delinsGA	ENSP00000512385.1:n.*14_*15delinsGA
ENST00000696090.1:c.*14_*15delinsGA	ENSP00000512386.1:n.*14_*15delinsGA
ENST00000696091.1:c.*14_*15delinsGA	ENSP00000512388.1:n.*14_*15delinsGA
ENST00000593537.1:c.647_648delinsGA	ENSP00000469455.1:n.647_648delinsGA
ENST00000599795.5:c.243+404_243+405delinsGA	ENSP00000470689.1:n.243+404_243+405delinsGA
NM_006179.4:c.*14_*15delinsGA	NP_006170.1:n.*14_*15delinsGA
XM_005258962.2:c.*14_*15delinsGA	XP_005259019.1:n.*14_*15delinsGA
XM_006723232.2:c.*14_*15delinsGA	XP_006723295.1:n.*14_*15delinsGA
XM_011527008.1:c.*14_*15delinsGA	XP_011525310.1:n.*14_*15delinsGA
XM_011527009.1:c.*14_*15delinsGA	XP_011525311.1:n.*14_*15delinsGA
XM_011527010.1:c.*14_*15delinsGA	XP_011525312.1:n.*14_*15delinsGA
XM_005258962.3:c.*14_*15delinsGA	XP_005259019.1:n.*14_*15delinsGA
XM_006723232.3:c.*14_*15delinsGA	XP_006723295.1:n.*14_*15delinsGA
XM_011527008.2:c.*14_*15delinsGA	XP_011525310.1:n.*14_*15delinsGA
XM_011527009.2:c.*14_*15delinsGA	XP_011525311.1:n.*14_*15delinsGA
XM_011527010.2:c.*14_*15delinsGA	XP_011525312.1:n.*14_*15delinsGA
XR_001753693.1:n.692_693delinsGA
XR_001753694.1:n.692_693delinsGA
NM_001395489.1:c.*14_*15delinsGA	NP_001382418.1:n.*14_*15delinsGA
NM_006179.5:c.*14_*15delinsGA MANE Select	NP_006170.1:n.*14_*15delinsGA