Canonical Allele Identifier: CA1200787267

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879262G= , CM000663.2:g.156879262G=	GRCh38
NC_000001.10:g.156849054G= , CM000663.1:g.156849054G=	GRCh37
NC_000001.9:g.155115678G=	NCBI36
NG_007493.1:g.68513G= , LRG_261:g.68513G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1766G=	ENSP00000502725.1:p.Arg589=
ENST00000392302.7:c.1766G=	ENSP00000376120.3:p.Arg589=
ENST00000497019.7:c.*538G=	ENSP00000436804.2:n.*538G=
ENST00000524377.7:c.1946G= MANE Select	ENSP00000431418.1:p.Arg649=
ENST00000674537.1:c.1766G=	ENSP00000502725.1:p.Arg589=
ENST00000358660.3:c.1937G=	ENSP00000351486.3:p.Arg646=
ENST00000368196.7:c.1928G=	ENSP00000357179.3:p.Arg643=
ENST00000392302.6:c.1838G=	ENSP00000376120.2:p.Arg613=
ENST00000497019.6:c.*538G=	ENSP00000436804.1:n.*538G=
ENST00000524377.5:c.1946G=	ENSP00000431418.1:p.Arg649=
ENST00000530298.5:n.2399G=
NM_001007792.1:c.1838G= , LRG_261t1:c.1838G=	NP_001007793.1:p.Arg613=
NM_001012331.1:c.1928G= , LRG_261t2:c.1928G=	NP_001012331.1:p.Arg643=
NM_002529.3:c.1946G= , LRG_261t3:c.1946G=	NP_002520.2:p.Arg649=
NM_001012331.2:c.1928G=	NP_001012331.1:p.Arg643=
NM_002529.4:c.1946G= MANE Select	NP_002520.2:p.Arg649=