Canonical Allele Identifier: CA309446675
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs34922845

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061579_49061580insT , CM000681.2:g.49061579_49061580insT GRCh38
NC_000019.9:g.49564836_49564837insT , CM000681.1:g.49564836_49564837insT GRCh37
NC_000019.8:g.54256648_54256649insT NCBI36
NG_016289.1:g.7288_7289insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000593537.2:c.418_419insA MANE Select ENSP00000469455.1:p.Arg140GlnfsTer5
ENST00000594938.2:c.418_419insA ENSP00000512387.1:p.Arg140GlnfsTer5
ENST00000595857.6:c.418_419insA ENSP00000471508.2:p.Arg140GlnfsTer5
ENST00000696088.1:c.418_419insA ENSP00000512384.1:p.Arg140GlnfsTer5
ENST00000696089.1:c.418_419insA ENSP00000512385.1:p.Arg140GlnfsTer5
ENST00000696090.1:c.418_419insA ENSP00000512386.1:p.Arg140GlnfsTer5
ENST00000696091.1:c.418_419insA ENSP00000512388.1:p.Arg140GlnfsTer5
ENST00000593537.1:c.418_419insA ENSP00000469455.1:p.Arg140GlnfsTer5
ENST00000595857.5:c.418_419insA ENSP00000471508.1:p.Arg140GlnfsTer?
ENST00000599795.5:c.243+175_243+176insA ENSP00000470689.1:n.243+175_243+176insA
NM_006179.4:c.418_419insA NP_006170.1:p.Arg140GlnfsTer5
XM_005258962.2:c.418_419insA XP_005259019.1:p.Arg140GlnfsTer5
XM_006723232.2:c.418_419insA XP_006723295.1:p.Arg140GlnfsTer5
XM_011527008.1:c.448_449insA XP_011525310.1:p.Arg150GlnfsTer5
XM_011527009.1:c.418_419insA XP_011525311.1:p.Arg140GlnfsTer5
XM_011527010.1:c.418_419insA XP_011525312.1:p.Arg140GlnfsTer5
XM_005258962.3:c.418_419insA XP_005259019.1:p.Arg140GlnfsTer5
XM_006723232.3:c.418_419insA XP_006723295.1:p.Arg140GlnfsTer5
XM_011527008.2:c.448_449insA XP_011525310.1:p.Arg150GlnfsTer5
XM_011527009.2:c.418_419insA XP_011525311.1:p.Arg140GlnfsTer5
XM_011527010.2:c.418_419insA XP_011525312.1:p.Arg140GlnfsTer5
XR_001753693.1:n.463_464insA
XR_001753694.1:n.463_464insA
NM_001395489.1:c.418_419insA NP_001382418.1:p.Arg140GlnfsTer5
NM_006179.5:c.418_419insA MANE Select NP_006170.1:p.Arg140GlnfsTer5