Canonical Allele Identifier: CA2648464053
Gene: NTRK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156876433_156876441dup , CM000663.2:g.156876433_156876441dup GRCh38
NC_000001.10:g.156846225_156846233dup , CM000663.1:g.156846225_156846233dup GRCh37
NC_000001.9:g.155112849_155112857dup NCBI36
NG_007493.1:g.65684_65692dup , LRG_261:g.65684_65692dup

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1486_1494dup ENSP00000502725.1:p.Gln498_Arg499insAspPheGln
ENST00000392302.7:c.1486_1494dup ENSP00000376120.3:p.Gln498_Arg499insAspPheGln
ENST00000497019.7:c.*258_*266dup ENSP00000436804.2:n.*258_*266dup
ENST00000524377.7:c.1666_1674dup MANE Select ENSP00000431418.1:p.Gln558_Arg559insAspPheGln
ENST00000674537.1:c.1486_1494dup ENSP00000502725.1:p.Gln498_Arg499insAspPheGln
ENST00000358660.3:c.1657_1665dup ENSP00000351486.3:p.Gln555_Arg556insAspPheGln
ENST00000368196.7:c.1648_1656dup ENSP00000357179.3:p.Gln552_Arg553insAspPheGln
ENST00000392302.6:c.1558_1566dup ENSP00000376120.2:p.Gln522_Arg523insAspPheGln
ENST00000497019.6:c.*258_*266dup ENSP00000436804.1:n.*258_*266dup
ENST00000524377.5:c.1666_1674dup ENSP00000431418.1:p.Gln558_Arg559insAspPheGln
ENST00000530298.5:n.2119_2127dup
NM_001007792.1:c.1558_1566dup , LRG_261t1:c.1558_1566dup NP_001007793.1:p.Gln522_Arg523insAspPheGln
NM_001012331.1:c.1648_1656dup , LRG_261t2:c.1648_1656dup NP_001012331.1:p.Gln552_Arg553insAspPheGln
NM_002529.3:c.1666_1674dup , LRG_261t3:c.1666_1674dup NP_002520.2:p.Gln558_Arg559insAspPheGln
NM_001012331.2:c.1648_1656dup NP_001012331.1:p.Gln552_Arg553insAspPheGln
NM_002529.4:c.1666_1674dup MANE Select NP_002520.2:p.Gln558_Arg559insAspPheGln