Canonical Allele Identifier: CA1200788683

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881490G= , CM000663.2:g.156881490G=	GRCh38
NC_000001.10:g.156851282G= , CM000663.1:g.156851282G=	GRCh37
NC_000001.9:g.155117906G=	NCBI36
NG_007493.1:g.70741G= , LRG_261:g.70741G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.2059G=	ENSP00000502725.1:p.Glu687=
ENST00000392302.7:c.2059G=	ENSP00000376120.3:p.Glu687=
ENST00000497019.7:c.*831G=	ENSP00000436804.2:n.*831G=
ENST00000524377.7:c.2239G= MANE Select	ENSP00000431418.1:p.Glu747=
ENST00000531606.2:c.298G=
ENST00000674537.1:c.2059G=	ENSP00000502725.1:p.Glu687=
ENST00000358660.3:c.2230G=	ENSP00000351486.3:p.Glu744=
ENST00000368196.7:c.2221G=	ENSP00000357179.3:p.Glu741=
ENST00000392302.6:c.2131G=	ENSP00000376120.2:p.Glu711=
ENST00000497019.6:c.*831G=	ENSP00000436804.1:n.*831G=
ENST00000524377.5:c.2239G=	ENSP00000431418.1:p.Glu747=
ENST00000530298.5:n.2692G=
ENST00000531606.1:n.282G=
NM_001007792.1:c.2131G= , LRG_261t1:c.2131G=	NP_001007793.1:p.Glu711=
NM_001012331.1:c.2221G= , LRG_261t2:c.2221G=	NP_001012331.1:p.Glu741=
NM_002529.3:c.2239G= , LRG_261t3:c.2239G=	NP_002520.2:p.Glu747=
NM_001012331.2:c.2221G=	NP_001012331.1:p.Glu741=
NM_002529.4:c.2239G= MANE Select	NP_002520.2:p.Glu747=