Canonical Allele Identifier: CA1008111759
Gene: NTRK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156881491_156881492insT , CM000663.2:g.156881491_156881492insT GRCh38
NC_000001.10:g.156851283_156851284insT , CM000663.1:g.156851283_156851284insT GRCh37
NC_000001.9:g.155117907_155117908insT NCBI36
NG_007493.1:g.70742_70743insT , LRG_261:g.70742_70743insT

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.2060_2061insT ENSP00000502725.1:p.Glu687AspfsTer?
ENST00000392302.7:c.2060_2061insT ENSP00000376120.3:p.Glu687AspfsTer?
ENST00000497019.7:c.*832_*833insT ENSP00000436804.2:n.*832_*833insT
ENST00000524377.7:c.2240_2241insT MANE Select ENSP00000431418.1:p.Glu747AspfsTer?
ENST00000531606.2:c.299_300insT
ENST00000674537.1:c.2060_2061insT ENSP00000502725.1:p.Glu687AspfsTer?
ENST00000358660.3:c.2231_2232insT ENSP00000351486.3:p.Glu744AspfsTer?
ENST00000368196.7:c.2222_2223insT ENSP00000357179.3:p.Glu741AspfsTer?
ENST00000392302.6:c.2132_2133insT ENSP00000376120.2:p.Glu711AspfsTer?
ENST00000497019.6:c.*832_*833insT ENSP00000436804.1:n.*832_*833insT
ENST00000524377.5:c.2240_2241insT ENSP00000431418.1:p.Glu747AspfsTer?
ENST00000530298.5:n.2693_2694insT
ENST00000531606.1:n.283_284insT
NM_001007792.1:c.2132_2133insT , LRG_261t1:c.2132_2133insT NP_001007793.1:p.Glu711AspfsTer?
NM_001012331.1:c.2222_2223insT , LRG_261t2:c.2222_2223insT NP_001012331.1:p.Glu741AspfsTer?
NM_002529.3:c.2240_2241insT , LRG_261t3:c.2240_2241insT NP_002520.2:p.Glu747AspfsTer?
NM_001012331.2:c.2222_2223insT NP_001012331.1:p.Glu741AspfsTer?
NM_002529.4:c.2240_2241insT MANE Select NP_002520.2:p.Glu747AspfsTer?