Canonical Allele Identifier: CA1143639385
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156876408G= , CM000663.2:g.156876408G= GRCh38
NC_000001.10:g.156846200G= , CM000663.1:g.156846200G= GRCh37
NC_000001.9:g.155112824G= NCBI36
NG_007493.1:g.65659G= , LRG_261:g.65659G=

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1461G= ENSP00000502725.1:p.Lys487=
ENST00000392302.7:c.1461G= ENSP00000376120.3:p.Lys487=
ENST00000497019.7:c.*233G= ENSP00000436804.2:n.*233G=
ENST00000524377.7:c.1641G= MANE Select ENSP00000431418.1:p.Lys547=
ENST00000674537.1:c.1461G= ENSP00000502725.1:p.Lys487=
ENST00000358660.3:c.1632G= ENSP00000351486.3:p.Lys544=
ENST00000368196.7:c.1623G= ENSP00000357179.3:p.Lys541=
ENST00000392302.6:c.1533G= ENSP00000376120.2:p.Lys511=
ENST00000497019.6:c.*233G= ENSP00000436804.1:n.*233G=
ENST00000524377.5:c.1641G= ENSP00000431418.1:p.Lys547=
ENST00000530298.5:n.2094G=
NM_001007792.1:c.1533G= , LRG_261t1:c.1533G= NP_001007793.1:p.Lys511=
NM_001012331.1:c.1623G= , LRG_261t2:c.1623G= NP_001012331.1:p.Lys541=
NM_002529.3:c.1641G= , LRG_261t3:c.1641G= NP_002520.2:p.Lys547=
NM_001012331.2:c.1623G= NP_001012331.1:p.Lys541=
NM_002529.4:c.1641G= MANE Select NP_002520.2:p.Lys547=