Canonical Allele Identifier: CA1200778799

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860962C= , CM000663.2:g.156860962C=	GRCh38
NC_000001.10:g.156830754C= , CM000663.1:g.156830754C=	GRCh37
NC_000001.9:g.155097378C=	NCBI36
NG_007493.1:g.50213C= , LRG_261:g.50213C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.51-3392C=	ENSP00000502725.1:n.51-3392C=
ENST00000392302.7:c.51-3392C=	ENSP00000376120.3:n.51-3392C=
ENST00000497019.7:c.51-3392C=	ENSP00000436804.2:n.51-3392C=
ENST00000524377.7:c.28C= MANE Select	ENSP00000431418.1:p.Leu10=
ENST00000674537.1:c.51-3392C=	ENSP00000502725.1:n.51-3392C=
ENST00000675461.1:c.28C=	ENSP00000501668.1:p.Leu10=
ENST00000358660.3:c.28C=	ENSP00000351486.3:p.Leu10=
ENST00000368196.7:c.28C=	ENSP00000357179.3:p.Leu10=
ENST00000392302.6:c.123-3392C=	ENSP00000376120.2:n.123-3392C=
ENST00000489021.6:n.313-12671C=
ENST00000497019.6:c.123-3392C=	ENSP00000436804.1:n.123-3392C=
ENST00000524377.5:c.28C=	ENSP00000431418.1:p.Leu10=
ENST00000530298.5:n.271-3392C=
ENST00000533630.1:n.50C=
NM_001007792.1:c.123-3392C= , LRG_261t1:c.123-3392C=	NP_001007793.1:n.123-3392C=
NM_001012331.1:c.28C= , LRG_261t2:c.28C=	NP_001012331.1:p.Leu10=
NM_002529.3:c.28C= , LRG_261t3:c.28C=	NP_002520.2:p.Leu10=
NM_001012331.2:c.28C=	NP_001012331.1:p.Leu10=
NM_002529.4:c.28C= MANE Select	NP_002520.2:p.Leu10=