Canonical Allele Identifier: CA1200785914

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876095A= , CM000663.2:g.156876095A=	GRCh38
NC_000001.10:g.156845887A= , CM000663.1:g.156845887A=	GRCh37
NC_000001.9:g.155112511A=	NCBI36
NG_007493.1:g.65346A= , LRG_261:g.65346A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1337A=	ENSP00000502725.1:p.Lys446=
ENST00000392302.7:c.1337A=	ENSP00000376120.3:p.Lys446=
ENST00000497019.7:c.*109A=	ENSP00000436804.2:n.*109A=
ENST00000524377.7:c.1517A= MANE Select	ENSP00000431418.1:p.Lys506=
ENST00000674537.1:c.1337A=	ENSP00000502725.1:p.Lys446=
ENST00000358660.3:c.1508A=	ENSP00000351486.3:p.Lys503=
ENST00000368196.7:c.1499A=	ENSP00000357179.3:p.Lys500=
ENST00000392302.6:c.1409A=	ENSP00000376120.2:p.Lys470=
ENST00000497019.6:c.*109A=	ENSP00000436804.1:n.*109A=
ENST00000524377.5:c.1517A=	ENSP00000431418.1:p.Lys506=
ENST00000530298.5:n.1970A=
ENST00000534682.1:n.740A=
NM_001007792.1:c.1409A= , LRG_261t1:c.1409A=	NP_001007793.1:p.Lys470=
NM_001012331.1:c.1499A= , LRG_261t2:c.1499A=	NP_001012331.1:p.Lys500=
NM_002529.3:c.1517A= , LRG_261t3:c.1517A=	NP_002520.2:p.Lys506=
NM_001012331.2:c.1499A=	NP_001012331.1:p.Lys500=
NM_002529.4:c.1517A= MANE Select	NP_002520.2:p.Lys506=