Canonical Allele Identifier: CA1200778691
Gene: NTRK1 HGNC NCBI

Linked Data

dbSNP Id: rs1655599108

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156860772_156860774del , CM000663.2:g.156860772_156860774del GRCh38
NC_000001.10:g.156830564_156830566del , CM000663.1:g.156830564_156830566del GRCh37
NC_000001.9:g.155097188_155097190del NCBI36
NG_007493.1:g.50023_50025del , LRG_261:g.50023_50025del

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.51-3582_51-3580del ENSP00000502725.1:n.51-3582_51-3580del
ENST00000392302.7:c.51-3582_51-3580del ENSP00000376120.3:n.51-3582_51-3580del
ENST00000497019.7:c.51-3582_51-3580del ENSP00000436804.2:n.51-3582_51-3580del
ENST00000674537.1:c.51-3582_51-3580del ENSP00000502725.1:n.51-3582_51-3580del
ENST00000392302.6:c.123-3582_123-3580del ENSP00000376120.2:n.123-3582_123-3580del
ENST00000489021.6:n.313-12861_313-12859del
ENST00000497019.6:c.123-3582_123-3580del ENSP00000436804.1:n.123-3582_123-3580del
ENST00000530298.5:n.271-3582_271-3580del
NM_001007792.1:c.123-3582_123-3580del , LRG_261t1:c.123-3582_123-3580del NP_001007793.1:n.123-3582_123-3580del