Canonical Allele Identifier: CA2746258029
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156860798_156860799insAGCCTGCT , CM000663.2:g.156860798_156860799insAGCCTGCT GRCh38
NC_000001.10:g.156830590_156830591insAGCCTGCT , CM000663.1:g.156830590_156830591insAGCCTGCT GRCh37
NC_000001.9:g.155097214_155097215insAGCCTGCT NCBI36
NG_007493.1:g.50049_50050insAGCCTGCT , LRG_261:g.50049_50050insAGCCTGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.51-3556_51-3555insAGCCTGCT ENSP00000502725.1:n.51-3556_51-3555insAGCCTGCT
ENST00000392302.7:c.51-3556_51-3555insAGCCTGCT ENSP00000376120.3:n.51-3556_51-3555insAGCCTGCT
ENST00000497019.7:c.51-3556_51-3555insAGCCTGCT ENSP00000436804.2:n.51-3556_51-3555insAGCCTGCT
ENST00000674537.1:c.51-3556_51-3555insAGCCTGCT ENSP00000502725.1:n.51-3556_51-3555insAGCCTGCT
ENST00000392302.6:c.123-3556_123-3555insAGCCTGCT ENSP00000376120.2:n.123-3556_123-3555insAGCCTGCT
ENST00000489021.6:n.313-12835_313-12834insAGCCTGCT
ENST00000497019.6:c.123-3556_123-3555insAGCCTGCT ENSP00000436804.1:n.123-3556_123-3555insAGCCTGCT
ENST00000530298.5:n.271-3556_271-3555insAGCCTGCT
NM_001007792.1:c.123-3556_123-3555insAGCCTGCT , LRG_261t1:c.123-3556_123-3555insAGCCTGCT NP_001007793.1:n.123-3556_123-3555insAGCCTGCT