Canonical Allele Identifier: CA889795505
Gene: NTRK1 HGNC NCBI

Linked Data

dbSNP Id: rs1195980491
gnomAD v3: 1-156860777-GA-G
gnomAD v4: 1-156860777-GA-G
MyVariant Identifiers: chr1:g.156830570del (hg19) chr1:g.156860778del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156860778del , CM000663.2:g.156860778del GRCh38
NC_000001.10:g.156830570del , CM000663.1:g.156830570del GRCh37
NC_000001.9:g.155097194del NCBI36
NG_007493.1:g.50029del , LRG_261:g.50029del

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.51-3576del ENSP00000502725.1:n.51-3576del
ENST00000392302.7:c.51-3576del ENSP00000376120.3:n.51-3576del
ENST00000497019.7:c.51-3576del ENSP00000436804.2:n.51-3576del
ENST00000674537.1:c.51-3576del ENSP00000502725.1:n.51-3576del
ENST00000392302.6:c.123-3576del ENSP00000376120.2:n.123-3576del
ENST00000489021.6:n.313-12855del
ENST00000497019.6:c.123-3576del ENSP00000436804.1:n.123-3576del
ENST00000530298.5:n.271-3576del
NM_001007792.1:c.123-3576del , LRG_261t1:c.123-3576del NP_001007793.1:n.123-3576del
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