Canonical Allele Identifier: CA1140762817

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881523G= , CM000663.2:g.156881523G=	GRCh38
NC_000001.10:g.156851315G= , CM000663.1:g.156851315G=	GRCh37
NC_000001.9:g.155117939G=	NCBI36
NG_007493.1:g.70774G= , LRG_261:g.70774G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2092G=	ENSP00000502725.1:p.Ala698=
ENST00000392302.7:c.2092G=	ENSP00000376120.3:p.Ala698=
ENST00000497019.7:c.*864G=	ENSP00000436804.2:n.*864G=
ENST00000524377.7:c.2272G= MANE Select	ENSP00000431418.1:p.Ala758=
ENST00000531606.2:c.331G=
ENST00000674537.1:c.2092G=	ENSP00000502725.1:p.Ala698=
ENST00000358660.3:c.2263G=	ENSP00000351486.3:p.Ala755=
ENST00000368196.7:c.2254G=	ENSP00000357179.3:p.Ala752=
ENST00000392302.6:c.2164G=	ENSP00000376120.2:p.Ala722=
ENST00000497019.6:c.*864G=	ENSP00000436804.1:n.*864G=
ENST00000524377.5:c.2272G=	ENSP00000431418.1:p.Ala758=
ENST00000530298.5:n.2725G=
ENST00000531606.1:n.315G=
NM_001007792.1:c.2164G= , LRG_261t1:c.2164G=	NP_001007793.1:p.Ala722=
NM_001012331.1:c.2254G= , LRG_261t2:c.2254G=	NP_001012331.1:p.Ala752=
NM_002529.3:c.2272G= , LRG_261t3:c.2272G=	NP_002520.2:p.Ala758=
NM_001012331.2:c.2254G=	NP_001012331.1:p.Ala752=
NM_002529.4:c.2272G= MANE Select	NP_002520.2:p.Ala758=