Canonical Allele Identifier: CA1200785916

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876098G= , CM000663.2:g.156876098G=	GRCh38
NC_000001.10:g.156845890G= , CM000663.1:g.156845890G=	GRCh37
NC_000001.9:g.155112514G=	NCBI36
NG_007493.1:g.65349G= , LRG_261:g.65349G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1340G=	ENSP00000502725.1:p.Arg447=
ENST00000392302.7:c.1340G=	ENSP00000376120.3:p.Arg447=
ENST00000497019.7:c.*112G=	ENSP00000436804.2:n.*112G=
ENST00000524377.7:c.1520G= MANE Select	ENSP00000431418.1:p.Arg507=
ENST00000674537.1:c.1340G=	ENSP00000502725.1:p.Arg447=
ENST00000358660.3:c.1511G=	ENSP00000351486.3:p.Arg504=
ENST00000368196.7:c.1502G=	ENSP00000357179.3:p.Arg501=
ENST00000392302.6:c.1412G=	ENSP00000376120.2:p.Arg471=
ENST00000497019.6:c.*112G=	ENSP00000436804.1:n.*112G=
ENST00000524377.5:c.1520G=	ENSP00000431418.1:p.Arg507=
ENST00000530298.5:n.1973G=
ENST00000534682.1:n.743G=
NM_001007792.1:c.1412G= , LRG_261t1:c.1412G=	NP_001007793.1:p.Arg471=
NM_001012331.1:c.1502G= , LRG_261t2:c.1502G=	NP_001012331.1:p.Arg501=
NM_002529.3:c.1520G= , LRG_261t3:c.1520G=	NP_002520.2:p.Arg507=
NM_001012331.2:c.1502G=	NP_001012331.1:p.Arg501=
NM_002529.4:c.1520G= MANE Select	NP_002520.2:p.Arg507=