Canonical Allele Identifier: CA1143794233

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156868232T= , CM000663.2:g.156868232T=	GRCh38
NC_000001.10:g.156838024T= , CM000663.1:g.156838024T=	GRCh37
NC_000001.9:g.155104648T=	NCBI36
NG_007493.1:g.57483T= , LRG_261:g.57483T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.395T=	ENSP00000502725.1:p.Met132=
ENST00000392302.7:c.395T=	ENSP00000376120.3:p.Met132=
ENST00000497019.7:c.395T=	ENSP00000436804.2:p.Met132=
ENST00000524377.7:c.557T= MANE Select	ENSP00000431418.1:p.Met186=
ENST00000674537.1:c.395T=	ENSP00000502725.1:p.Met132=
ENST00000358660.3:c.557T=	ENSP00000351486.3:p.Met186=
ENST00000368196.7:c.557T=	ENSP00000357179.3:p.Met186=
ENST00000392302.6:c.467T=	ENSP00000376120.2:p.Met156=
ENST00000489021.6:n.313-5401T=
ENST00000497019.6:c.467T=	ENSP00000436804.1:p.Met156=
ENST00000524377.5:c.557T=	ENSP00000431418.1:p.Met186=
ENST00000530298.5:n.615T=
NM_001007792.1:c.467T= , LRG_261t1:c.467T=	NP_001007793.1:p.Met156=
NM_001012331.1:c.557T= , LRG_261t2:c.557T=	NP_001012331.1:p.Met186=
NM_002529.3:c.557T= , LRG_261t3:c.557T=	NP_002520.2:p.Met186=
NM_001012331.2:c.557T=	NP_001012331.1:p.Met186=
NM_002529.4:c.557T= MANE Select	NP_002520.2:p.Met186=