Canonical Allele Identifier: CA1200786084

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876413C= , CM000663.2:g.156876413C=	GRCh38
NC_000001.10:g.156846205C= , CM000663.1:g.156846205C=	GRCh37
NC_000001.9:g.155112829C=	NCBI36
NG_007493.1:g.65664C= , LRG_261:g.65664C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1466C=	ENSP00000502725.1:p.Ala489=
ENST00000392302.7:c.1466C=	ENSP00000376120.3:p.Ala489=
ENST00000497019.7:c.*238C=	ENSP00000436804.2:n.*238C=
ENST00000524377.7:c.1646C= MANE Select	ENSP00000431418.1:p.Ala549=
ENST00000674537.1:c.1466C=	ENSP00000502725.1:p.Ala489=
ENST00000358660.3:c.1637C=	ENSP00000351486.3:p.Ala546=
ENST00000368196.7:c.1628C=	ENSP00000357179.3:p.Ala543=
ENST00000392302.6:c.1538C=	ENSP00000376120.2:p.Ala513=
ENST00000497019.6:c.*238C=	ENSP00000436804.1:n.*238C=
ENST00000524377.5:c.1646C=	ENSP00000431418.1:p.Ala549=
ENST00000530298.5:n.2099C=
NM_001007792.1:c.1538C= , LRG_261t1:c.1538C=	NP_001007793.1:p.Ala513=
NM_001012331.1:c.1628C= , LRG_261t2:c.1628C=	NP_001012331.1:p.Ala543=
NM_002529.3:c.1646C= , LRG_261t3:c.1646C=	NP_002520.2:p.Ala549=
NM_001012331.2:c.1628C=	NP_001012331.1:p.Ala543=
NM_002529.4:c.1646C= MANE Select	NP_002520.2:p.Ala549=