Canonical Allele Identifier: CA2586964226
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156876419del , CM000663.2:g.156876419del GRCh38
NC_000001.10:g.156846211del , CM000663.1:g.156846211del GRCh37
NC_000001.9:g.155112835del NCBI36
NG_007493.1:g.65670del , LRG_261:g.65670del

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1472del ENSP00000502725.1:p.Glu491GlyfsTer?
ENST00000392302.7:c.1472del ENSP00000376120.3:p.Glu491GlyfsTer?
ENST00000497019.7:c.*244del ENSP00000436804.2:n.*244del
ENST00000524377.7:c.1652del MANE Select ENSP00000431418.1:p.Glu551GlyfsTer?
ENST00000674537.1:c.1472del ENSP00000502725.1:p.Glu491GlyfsTer?
ENST00000358660.3:c.1643del ENSP00000351486.3:p.Glu548GlyfsTer?
ENST00000368196.7:c.1634del ENSP00000357179.3:p.Glu545GlyfsTer?
ENST00000392302.6:c.1544del ENSP00000376120.2:p.Glu515GlyfsTer?
ENST00000497019.6:c.*244del ENSP00000436804.1:n.*244del
ENST00000524377.5:c.1652del ENSP00000431418.1:p.Glu551GlyfsTer?
ENST00000530298.5:n.2105del
NM_001007792.1:c.1544del , LRG_261t1:c.1544del NP_001007793.1:p.Glu515GlyfsTer?
NM_001012331.1:c.1634del , LRG_261t2:c.1634del NP_001012331.1:p.Glu545GlyfsTer?
NM_002529.3:c.1652del , LRG_261t3:c.1652del NP_002520.2:p.Glu551GlyfsTer?
NM_001012331.2:c.1634del NP_001012331.1:p.Glu545GlyfsTer?
NM_002529.4:c.1652del MANE Select NP_002520.2:p.Glu551GlyfsTer?