Canonical Allele Identifier: CA1141188060

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879336G= , CM000663.2:g.156879336G=	GRCh38
NC_000001.10:g.156849128G= , CM000663.1:g.156849128G=	GRCh37
NC_000001.9:g.155115752G=	NCBI36
NG_007493.1:g.68587G= , LRG_261:g.68587G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1840G=	ENSP00000502725.1:p.Asp614=
ENST00000392302.7:c.1840G=	ENSP00000376120.3:p.Asp614=
ENST00000497019.7:c.*612G=	ENSP00000436804.2:n.*612G=
ENST00000524377.7:c.2020G= MANE Select	ENSP00000431418.1:p.Asp674=
ENST00000674537.1:c.1840G=	ENSP00000502725.1:p.Asp614=
ENST00000358660.3:c.2011G=	ENSP00000351486.3:p.Asp671=
ENST00000368196.7:c.2002G=	ENSP00000357179.3:p.Asp668=
ENST00000392302.6:c.1912G=	ENSP00000376120.2:p.Asp638=
ENST00000497019.6:c.*612G=	ENSP00000436804.1:n.*612G=
ENST00000524377.5:c.2020G=	ENSP00000431418.1:p.Asp674=
ENST00000530298.5:n.2473G=
NM_001007792.1:c.1912G= , LRG_261t1:c.1912G=	NP_001007793.1:p.Asp638=
NM_001012331.1:c.2002G= , LRG_261t2:c.2002G=	NP_001012331.1:p.Asp668=
NM_002529.3:c.2020G= , LRG_261t3:c.2020G=	NP_002520.2:p.Asp674=
NM_001012331.2:c.2002G=	NP_001012331.1:p.Asp668=
NM_002529.4:c.2020G= MANE Select	NP_002520.2:p.Asp674=