Canonical Allele Identifier: CA1200788837

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881552G= , CM000663.2:g.156881552G=	GRCh38
NC_000001.10:g.156851344G= , CM000663.1:g.156851344G=	GRCh37
NC_000001.9:g.155117968G=	NCBI36
NG_007493.1:g.70803G= , LRG_261:g.70803G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2121G=	ENSP00000502725.1:p.Glu707=
ENST00000392302.7:c.2121G=	ENSP00000376120.3:p.Glu707=
ENST00000497019.7:c.*893G=	ENSP00000436804.2:n.*893G=
ENST00000524377.7:c.2301G= MANE Select	ENSP00000431418.1:p.Glu767=
ENST00000531606.2:c.360G=
ENST00000674537.1:c.2121G=	ENSP00000502725.1:p.Glu707=
ENST00000358660.3:c.2292G=	ENSP00000351486.3:p.Glu764=
ENST00000368196.7:c.2283G=	ENSP00000357179.3:p.Glu761=
ENST00000392302.6:c.2193G=	ENSP00000376120.2:p.Glu731=
ENST00000497019.6:c.*893G=	ENSP00000436804.1:n.*893G=
ENST00000524377.5:c.2301G=	ENSP00000431418.1:p.Glu767=
ENST00000530298.5:n.2754G=
ENST00000531606.1:n.344G=
NM_001007792.1:c.2193G= , LRG_261t1:c.2193G=	NP_001007793.1:p.Glu731=
NM_001012331.1:c.2283G= , LRG_261t2:c.2283G=	NP_001012331.1:p.Glu761=
NM_002529.3:c.2301G= , LRG_261t3:c.2301G=	NP_002520.2:p.Glu767=
NM_001012331.2:c.2283G=	NP_001012331.1:p.Glu761=
NM_002529.4:c.2301G= MANE Select	NP_002520.2:p.Glu767=