Canonical Allele Identifier: CA1139773137

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879126C= , CM000663.2:g.156879126C=	GRCh38
NC_000001.10:g.156848918C= , CM000663.1:g.156848918C=	GRCh37
NC_000001.9:g.155115542C=	NCBI36
NG_007493.1:g.68377C= , LRG_261:g.68377C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1630C=	ENSP00000502725.1:p.His544=
ENST00000392302.7:c.1630C=	ENSP00000376120.3:p.His544=
ENST00000497019.7:c.*402C=	ENSP00000436804.2:n.*402C=
ENST00000524377.7:c.1810C= MANE Select	ENSP00000431418.1:p.His604=
ENST00000674537.1:c.1630C=	ENSP00000502725.1:p.His544=
ENST00000358660.3:c.1801C=	ENSP00000351486.3:p.His601=
ENST00000368196.7:c.1792C=	ENSP00000357179.3:p.His598=
ENST00000392302.6:c.1702C=	ENSP00000376120.2:p.His568=
ENST00000497019.6:c.*402C=	ENSP00000436804.1:n.*402C=
ENST00000524377.5:c.1810C=	ENSP00000431418.1:p.His604=
ENST00000530298.5:n.2263C=
NM_001007792.1:c.1702C= , LRG_261t1:c.1702C=	NP_001007793.1:p.His568=
NM_001012331.1:c.1792C= , LRG_261t2:c.1792C=	NP_001012331.1:p.His598=
NM_002529.3:c.1810C= , LRG_261t3:c.1810C=	NP_002520.2:p.His604=
NM_001012331.2:c.1792C=	NP_001012331.1:p.His598=
NM_002529.4:c.1810C= MANE Select	NP_002520.2:p.His604=