Canonical Allele Identifier: CA342929761
Gene: NTRK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 526732
ClinVar RCV Id: RCV000631335
dbSNP Id: rs1553260399

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156861074G>C , CM000663.2:g.156861074G>C GRCh38
NC_000001.10:g.156830866G>C , CM000663.1:g.156830866G>C GRCh37
NC_000001.9:g.155097490G>C NCBI36
NG_007493.1:g.50325G>C , LRG_261:g.50325G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.51-3280G>C ENSP00000502725.1:n.51-3280G>C
ENST00000392302.7:c.51-3280G>C ENSP00000376120.3:n.51-3280G>C
ENST00000497019.7:c.51-3280G>C ENSP00000436804.2:n.51-3280G>C
ENST00000524377.7:c.140G>C MANE Select ENSP00000431418.1:p.Gly47Ala
ENST00000674537.1:c.51-3280G>C ENSP00000502725.1:n.51-3280G>C
ENST00000675461.1:c.140G>C ENSP00000501668.1:p.Gly47Ala
ENST00000358660.3:c.140G>C ENSP00000351486.3:p.Gly47Ala
ENST00000368196.7:c.140G>C ENSP00000357179.3:p.Gly47Ala
ENST00000392302.6:c.123-3280G>C ENSP00000376120.2:n.123-3280G>C
ENST00000489021.6:n.313-12559G>C
ENST00000497019.6:c.123-3280G>C ENSP00000436804.1:n.123-3280G>C
ENST00000524377.5:c.140G>C ENSP00000431418.1:p.Gly47Ala
ENST00000530298.5:n.271-3280G>C
ENST00000533630.1:n.162G>C
NM_001007792.1:c.123-3280G>C , LRG_261t1:c.123-3280G>C NP_001007793.1:n.123-3280G>C
NM_001012331.1:c.140G>C , LRG_261t2:c.140G>C NP_001012331.1:p.Gly47Ala
NM_002529.3:c.140G>C , LRG_261t3:c.140G>C NP_002520.2:p.Gly47Ala
NM_001012331.2:c.140G>C NP_001012331.1:p.Gly47Ala
NM_002529.4:c.140G>C MANE Select NP_002520.2:p.Gly47Ala