Canonical Allele Identifier: CA1200788866

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881566A= , CM000663.2:g.156881566A=	GRCh38
NC_000001.10:g.156851358A= , CM000663.1:g.156851358A=	GRCh37
NC_000001.9:g.155117982A=	NCBI36
NG_007493.1:g.70817A= , LRG_261:g.70817A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2135A=	ENSP00000502725.1:p.His712=
ENST00000392302.7:c.2135A=	ENSP00000376120.3:p.His712=
ENST00000497019.7:c.*907A=	ENSP00000436804.2:n.*907A=
ENST00000524377.7:c.2315A= MANE Select	ENSP00000431418.1:p.His772=
ENST00000531606.2:c.374A=
ENST00000674537.1:c.2135A=	ENSP00000502725.1:p.His712=
ENST00000358660.3:c.2306A=	ENSP00000351486.3:p.His769=
ENST00000368196.7:c.2297A=	ENSP00000357179.3:p.His766=
ENST00000392302.6:c.2207A=	ENSP00000376120.2:p.His736=
ENST00000497019.6:c.*907A=	ENSP00000436804.1:n.*907A=
ENST00000524377.5:c.2315A=	ENSP00000431418.1:p.His772=
ENST00000530298.5:n.2768A=
ENST00000531606.1:n.358A=
NM_001007792.1:c.2207A= , LRG_261t1:c.2207A=	NP_001007793.1:p.His736=
NM_001012331.1:c.2297A= , LRG_261t2:c.2297A=	NP_001012331.1:p.His766=
NM_002529.3:c.2315A= , LRG_261t3:c.2315A=	NP_002520.2:p.His772=
NM_001012331.2:c.2297A=	NP_001012331.1:p.His766=
NM_002529.4:c.2315A= MANE Select	NP_002520.2:p.His772=