Canonical Allele Identifier: CA342937930

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156845914A>T (hg19) ; chr1:g.156876122A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876122A>T , CM000663.2:g.156876122A>T	GRCh38
NC_000001.10:g.156845914A>T , CM000663.1:g.156845914A>T	GRCh37
NC_000001.9:g.155112538A>T	NCBI36
NG_007493.1:g.65373A>T , LRG_261:g.65373A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1364A>T	ENSP00000502725.1:p.Glu455Val
ENST00000392302.7:c.1364A>T	ENSP00000376120.3:p.Glu455Val
ENST00000497019.7:c.*136A>T	ENSP00000436804.2:n.*136A>T
ENST00000524377.7:c.1544A>T MANE Select	ENSP00000431418.1:p.Glu515Val
ENST00000674537.1:c.1364A>T	ENSP00000502725.1:p.Glu455Val
ENST00000358660.3:c.1535A>T	ENSP00000351486.3:p.Glu512Val
ENST00000368196.7:c.1526A>T	ENSP00000357179.3:p.Glu509Val
ENST00000392302.6:c.1436A>T	ENSP00000376120.2:p.Glu479Val
ENST00000497019.6:c.*136A>T	ENSP00000436804.1:n.*136A>T
ENST00000524377.5:c.1544A>T	ENSP00000431418.1:p.Glu515Val
ENST00000530298.5:n.1997A>T
ENST00000534682.1:n.767A>T
NM_001007792.1:c.1436A>T , LRG_261t1:c.1436A>T	NP_001007793.1:p.Glu479Val
NM_001012331.1:c.1526A>T , LRG_261t2:c.1526A>T	NP_001012331.1:p.Glu509Val
NM_002529.3:c.1544A>T , LRG_261t3:c.1544A>T	NP_002520.2:p.Glu515Val
NM_001012331.2:c.1526A>T	NP_001012331.1:p.Glu509Val
NM_002529.4:c.1544A>T MANE Select	NP_002520.2:p.Glu515Val