Canonical Allele Identifier: CA342932535
Gene: NTRK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156864739A>G , CM000663.2:g.156864739A>G GRCh38
NC_000001.10:g.156834531A>G , CM000663.1:g.156834531A>G GRCh37
NC_000001.9:g.155101155A>G NCBI36
NG_007493.1:g.53990A>G , LRG_261:g.53990A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.137A>G ENSP00000502725.1:p.Lys46Arg
ENST00000392302.7:c.137A>G ENSP00000376120.3:p.Lys46Arg
ENST00000497019.7:c.137A>G ENSP00000436804.2:p.Lys46Arg
ENST00000524377.7:c.299A>G MANE Select ENSP00000431418.1:p.Lys100Arg
ENST00000674537.1:c.137A>G ENSP00000502725.1:p.Lys46Arg
ENST00000675461.1:c.299A>G ENSP00000501668.1:p.Lys100Arg
ENST00000358660.3:c.299A>G ENSP00000351486.3:p.Lys100Arg
ENST00000368196.7:c.299A>G ENSP00000357179.3:p.Lys100Arg
ENST00000392302.6:c.209A>G ENSP00000376120.2:p.Lys70Arg
ENST00000489021.6:n.313-8894A>G
ENST00000497019.6:c.209A>G ENSP00000436804.1:p.Lys70Arg
ENST00000524377.5:c.299A>G ENSP00000431418.1:p.Lys100Arg
ENST00000530298.5:n.357A>G
ENST00000533630.1:n.321A>G
NM_001007792.1:c.209A>G , LRG_261t1:c.209A>G NP_001007793.1:p.Lys70Arg
NM_001012331.1:c.299A>G , LRG_261t2:c.299A>G NP_001012331.1:p.Lys100Arg
NM_002529.3:c.299A>G , LRG_261t3:c.299A>G NP_002520.2:p.Lys100Arg
NM_001012331.2:c.299A>G NP_001012331.1:p.Lys100Arg
NM_002529.4:c.299A>G MANE Select NP_002520.2:p.Lys100Arg