Canonical Allele Identifier: CA1200785933

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876147G= , CM000663.2:g.156876147G=	GRCh38
NC_000001.10:g.156845939G= , CM000663.1:g.156845939G=	GRCh37
NC_000001.9:g.155112563G=	NCBI36
NG_007493.1:g.65398G= , LRG_261:g.65398G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1389G=	ENSP00000502725.1:p.Lys463=
ENST00000392302.7:c.1389G=	ENSP00000376120.3:p.Lys463=
ENST00000497019.7:c.*161G=	ENSP00000436804.2:n.*161G=
ENST00000524377.7:c.1569G= MANE Select	ENSP00000431418.1:p.Lys523=
ENST00000674537.1:c.1389G=	ENSP00000502725.1:p.Lys463=
ENST00000358660.3:c.1560G=	ENSP00000351486.3:p.Lys520=
ENST00000368196.7:c.1551G=	ENSP00000357179.3:p.Lys517=
ENST00000392302.6:c.1461G=	ENSP00000376120.2:p.Lys487=
ENST00000497019.6:c.*161G=	ENSP00000436804.1:n.*161G=
ENST00000524377.5:c.1569G=	ENSP00000431418.1:p.Lys523=
ENST00000530298.5:n.2022G=
ENST00000534682.1:n.792G=
NM_001007792.1:c.1461G= , LRG_261t1:c.1461G=	NP_001007793.1:p.Lys487=
NM_001012331.1:c.1551G= , LRG_261t2:c.1551G=	NP_001012331.1:p.Lys517=
NM_002529.3:c.1569G= , LRG_261t3:c.1569G=	NP_002520.2:p.Lys523=
NM_001012331.2:c.1551G=	NP_001012331.1:p.Lys517=
NM_002529.4:c.1569G= MANE Select	NP_002520.2:p.Lys523=