Canonical Allele Identifier: CA1200778758

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860879T= , CM000663.2:g.156860879T=	GRCh38
NC_000001.10:g.156830671T= , CM000663.1:g.156830671T=	GRCh37
NC_000001.9:g.155097295T=	NCBI36
NG_007493.1:g.50130T= , LRG_261:g.50130T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.51-3475T=	ENSP00000502725.1:n.51-3475T=
ENST00000392302.7:c.51-3475T=	ENSP00000376120.3:n.51-3475T=
ENST00000497019.7:c.51-3475T=	ENSP00000436804.2:n.51-3475T=
ENST00000524377.7:c.-56T= MANE Select	ENSP00000431418.1:n.-56T=
ENST00000674537.1:c.51-3475T=	ENSP00000502725.1:n.51-3475T=
ENST00000368196.7:c.-56T=	ENSP00000357179.3:n.-56T=
ENST00000392302.6:c.123-3475T=	ENSP00000376120.2:n.123-3475T=
ENST00000489021.6:n.313-12754T=
ENST00000497019.6:c.123-3475T=	ENSP00000436804.1:n.123-3475T=
ENST00000530298.5:n.271-3475T=
NM_001007792.1:c.123-3475T= , LRG_261t1:c.123-3475T=	NP_001007793.1:n.123-3475T=
NM_001012331.1:c.-56T= , LRG_261t2:c.-56T=	NP_001012331.1:n.-56T=
NM_002529.3:c.-56T= , LRG_261t3:c.-56T=	NP_002520.2:n.-56T=
NM_001012331.2:c.-56T=	NP_001012331.1:n.-56T=
NM_002529.4:c.-56T= MANE Select	NP_002520.2:n.-56T=