Canonical Allele Identifier: CA1200782072

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156868125G= , CM000663.2:g.156868125G=	GRCh38
NC_000001.10:g.156837917G= , CM000663.1:g.156837917G=	GRCh37
NC_000001.9:g.155104541G=	NCBI36
NG_007493.1:g.57376G= , LRG_261:g.57376G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.288G=	ENSP00000502725.1:p.Leu96=
ENST00000392302.7:c.288G=	ENSP00000376120.3:p.Leu96=
ENST00000497019.7:c.288G=	ENSP00000436804.2:p.Leu96=
ENST00000524377.7:c.450G= MANE Select	ENSP00000431418.1:p.Leu150=
ENST00000674537.1:c.288G=	ENSP00000502725.1:p.Leu96=
ENST00000358660.3:c.450G=	ENSP00000351486.3:p.Leu150=
ENST00000368196.7:c.450G=	ENSP00000357179.3:p.Leu150=
ENST00000392302.6:c.360G=	ENSP00000376120.2:p.Leu120=
ENST00000489021.6:n.313-5508G=
ENST00000497019.6:c.360G=	ENSP00000436804.1:p.Leu120=
ENST00000524377.5:c.450G=	ENSP00000431418.1:p.Leu150=
ENST00000530298.5:n.508G=
NM_001007792.1:c.360G= , LRG_261t1:c.360G=	NP_001007793.1:p.Leu120=
NM_001012331.1:c.450G= , LRG_261t2:c.450G=	NP_001012331.1:p.Leu150=
NM_002529.3:c.450G= , LRG_261t3:c.450G=	NP_002520.2:p.Leu150=
NM_001012331.2:c.450G=	NP_001012331.1:p.Leu150=
NM_002529.4:c.450G= MANE Select	NP_002520.2:p.Leu150=