Canonical Allele Identifier: CA342938410
Gene: NTRK1 HGNC NCBI

Linked Data

dbSNP Id: rs2102919088

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156876412G>C , CM000663.2:g.156876412G>C GRCh38
NC_000001.10:g.156846204G>C , CM000663.1:g.156846204G>C GRCh37
NC_000001.9:g.155112828G>C NCBI36
NG_007493.1:g.65663G>C , LRG_261:g.65663G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1465G>C ENSP00000502725.1:p.Ala489Pro
ENST00000392302.7:c.1465G>C ENSP00000376120.3:p.Ala489Pro
ENST00000497019.7:c.*237G>C ENSP00000436804.2:n.*237G>C
ENST00000524377.7:c.1645G>C MANE Select ENSP00000431418.1:p.Ala549Pro
ENST00000674537.1:c.1465G>C ENSP00000502725.1:p.Ala489Pro
ENST00000358660.3:c.1636G>C ENSP00000351486.3:p.Ala546Pro
ENST00000368196.7:c.1627G>C ENSP00000357179.3:p.Ala543Pro
ENST00000392302.6:c.1537G>C ENSP00000376120.2:p.Ala513Pro
ENST00000497019.6:c.*237G>C ENSP00000436804.1:n.*237G>C
ENST00000524377.5:c.1645G>C ENSP00000431418.1:p.Ala549Pro
ENST00000530298.5:n.2098G>C
NM_001007792.1:c.1537G>C , LRG_261t1:c.1537G>C NP_001007793.1:p.Ala513Pro
NM_001012331.1:c.1627G>C , LRG_261t2:c.1627G>C NP_001012331.1:p.Ala543Pro
NM_002529.3:c.1645G>C , LRG_261t3:c.1645G>C NP_002520.2:p.Ala549Pro
NM_001012331.2:c.1627G>C NP_001012331.1:p.Ala543Pro
NM_002529.4:c.1645G>C MANE Select NP_002520.2:p.Ala549Pro