Canonical Allele Identifier: CA1008110707
Gene: NTRK1 HGNC NCBI

Linked Data

dbSNP Id: rs1655602844

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156860843_156860844del , CM000663.2:g.156860843_156860844del GRCh38
NC_000001.10:g.156830635_156830636del , CM000663.1:g.156830635_156830636del GRCh37
NC_000001.9:g.155097259_155097260del NCBI36
NG_007493.1:g.50094_50095del , LRG_261:g.50094_50095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.51-3511_51-3510del ENSP00000502725.1:n.51-3511_51-3510del
ENST00000392302.7:c.51-3511_51-3510del ENSP00000376120.3:n.51-3511_51-3510del
ENST00000497019.7:c.51-3511_51-3510del ENSP00000436804.2:n.51-3511_51-3510del
ENST00000674537.1:c.51-3511_51-3510del ENSP00000502725.1:n.51-3511_51-3510del
ENST00000368196.7:c.-92_-91del ENSP00000357179.3:n.-92_-91del
ENST00000392302.6:c.123-3511_123-3510del ENSP00000376120.2:n.123-3511_123-3510del
ENST00000489021.6:n.313-12790_313-12789del
ENST00000497019.6:c.123-3511_123-3510del ENSP00000436804.1:n.123-3511_123-3510del
ENST00000530298.5:n.271-3511_271-3510del
NM_001007792.1:c.123-3511_123-3510del , LRG_261t1:c.123-3511_123-3510del NP_001007793.1:n.123-3511_123-3510del