Canonical Allele Identifier: CA1200785955

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876210G= , CM000663.2:g.156876210G=	GRCh38
NC_000001.10:g.156846002G= , CM000663.1:g.156846002G=	GRCh37
NC_000001.9:g.155112626G=	NCBI36
NG_007493.1:g.65461G= , LRG_261:g.65461G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1452G=	ENSP00000502725.1:p.Lys484=
ENST00000392302.7:c.1452G=	ENSP00000376120.3:p.Lys484=
ENST00000497019.7:c.*224G=	ENSP00000436804.2:n.*224G=
ENST00000524377.7:c.1632G= MANE Select	ENSP00000431418.1:p.Lys544=
ENST00000674537.1:c.1452G=	ENSP00000502725.1:p.Lys484=
ENST00000358660.3:c.1623G=	ENSP00000351486.3:p.Lys541=
ENST00000368196.7:c.1614G=	ENSP00000357179.3:p.Lys538=
ENST00000392302.6:c.1524G=	ENSP00000376120.2:p.Lys508=
ENST00000497019.6:c.*224G=	ENSP00000436804.1:n.*224G=
ENST00000524377.5:c.1632G=	ENSP00000431418.1:p.Lys544=
ENST00000530298.5:n.2085G=
NM_001007792.1:c.1524G= , LRG_261t1:c.1524G=	NP_001007793.1:p.Lys508=
NM_001012331.1:c.1614G= , LRG_261t2:c.1614G=	NP_001012331.1:p.Lys538=
NM_002529.3:c.1632G= , LRG_261t3:c.1632G=	NP_002520.2:p.Lys544=
NM_001012331.2:c.1614G=	NP_001012331.1:p.Lys538=
NM_002529.4:c.1632G= MANE Select	NP_002520.2:p.Lys544=