Canonical Allele Identifier: CA1200785890
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156876029C= , CM000663.2:g.156876029C= GRCh38
NC_000001.10:g.156845821C= , CM000663.1:g.156845821C= GRCh37
NC_000001.9:g.155112445C= NCBI36
NG_007493.1:g.65280C= , LRG_261:g.65280C=

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1322-51C= ENSP00000502725.1:n.1322-51C=
ENST00000392302.7:c.1322-51C= ENSP00000376120.3:n.1322-51C=
ENST00000497019.7:c.*94-51C= ENSP00000436804.2:n.*94-51C=
ENST00000524377.7:c.1502-51C= MANE Select ENSP00000431418.1:n.1502-51C=
ENST00000674537.1:c.1322-51C= ENSP00000502725.1:n.1322-51C=
ENST00000358660.3:c.1484-42C= ENSP00000351486.3:n.1484-42C=
ENST00000368196.7:c.1484-51C= ENSP00000357179.3:n.1484-51C=
ENST00000392302.6:c.1394-51C= ENSP00000376120.2:n.1394-51C=
ENST00000497019.6:c.*94-51C= ENSP00000436804.1:n.*94-51C=
ENST00000524377.5:c.1502-51C= ENSP00000431418.1:n.1502-51C=
ENST00000530298.5:n.1904C=
ENST00000534682.1:n.725-51C=
NM_001007792.1:c.1394-51C= , LRG_261t1:c.1394-51C= NP_001007793.1:n.1394-51C=
NM_001012331.1:c.1484-51C= , LRG_261t2:c.1484-51C= NP_001012331.1:n.1484-51C=
NM_002529.3:c.1502-51C= , LRG_261t3:c.1502-51C= NP_002520.2:n.1502-51C=
NM_001012331.2:c.1484-51C= NP_001012331.1:n.1484-51C=
NM_002529.4:c.1502-51C= MANE Select NP_002520.2:n.1502-51C=