Canonical Allele Identifier: CA256294
Gene: NTRK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12311
dbSNP Id: rs121964869

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156873858A>G , CM000663.2:g.156873858A>G GRCh38
NC_000001.10:g.156843650A>G , CM000663.1:g.156843650A>G GRCh37
NC_000001.9:g.155110274A>G NCBI36
NG_007493.1:g.63109A>G , LRG_261:g.63109A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.914A>G ENSP00000502725.1:p.Tyr305Cys
ENST00000392302.7:c.914A>G ENSP00000376120.3:p.Tyr305Cys
ENST00000497019.7:c.781A>G ENSP00000436804.2:p.Thr261Ala
ENST00000524377.7:c.1076A>G MANE Select ENSP00000431418.1:p.Tyr359Cys
ENST00000674537.1:c.914A>G ENSP00000502725.1:p.Tyr305Cys
ENST00000358660.3:c.1076A>G ENSP00000351486.3:p.Tyr359Cys
ENST00000368196.7:c.1076A>G ENSP00000357179.3:p.Tyr359Cys
ENST00000392302.6:c.986A>G ENSP00000376120.2:p.Tyr329Cys
ENST00000489021.6:n.538A>G
ENST00000497019.6:c.853A>G ENSP00000436804.1:p.Thr285Ala
ENST00000524377.5:c.1076A>G ENSP00000431418.1:p.Tyr359Cys
ENST00000530298.5:n.1134A>G
NM_001007792.1:c.986A>G , LRG_261t1:c.986A>G NP_001007793.1:p.Tyr329Cys
NM_001012331.1:c.1076A>G , LRG_261t2:c.1076A>G NP_001012331.1:p.Tyr359Cys
NM_002529.3:c.1076A>G , LRG_261t3:c.1076A>G NP_002520.2:p.Tyr359Cys
NM_001012331.2:c.1076A>G NP_001012331.1:p.Tyr359Cys
NM_002529.4:c.1076A>G MANE Select NP_002520.2:p.Tyr359Cys