Canonical Allele Identifier: CA16603452
Gene: NTRK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 382766
dbSNP Id: rs1057521447

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156880019G>A , CM000663.2:g.156880019G>A GRCh38
NC_000001.10:g.156849811G>A , CM000663.1:g.156849811G>A GRCh37
NC_000001.9:g.155116435G>A NCBI36
NG_007493.1:g.69270G>A , LRG_261:g.69270G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1887G>A ENSP00000502725.1:p.Leu629=
ENST00000392302.7:c.1887G>A ENSP00000376120.3:p.Leu629=
ENST00000497019.7:c.*659G>A ENSP00000436804.2:n.*659G>A
ENST00000524377.7:c.2067G>A MANE Select ENSP00000431418.1:p.Leu689=
ENST00000531606.2:c.35G>A
ENST00000674537.1:c.1887G>A ENSP00000502725.1:p.Leu629=
ENST00000358660.3:c.2058G>A ENSP00000351486.3:p.Leu686=
ENST00000368196.7:c.2049G>A ENSP00000357179.3:p.Leu683=
ENST00000392302.6:c.1959G>A ENSP00000376120.2:p.Leu653=
ENST00000497019.6:c.*659G>A ENSP00000436804.1:n.*659G>A
ENST00000524377.5:c.2067G>A ENSP00000431418.1:p.Leu689=
ENST00000530298.5:n.2520G>A
ENST00000531606.1:n.19G>A
NM_001007792.1:c.1959G>A , LRG_261t1:c.1959G>A NP_001007793.1:p.Leu653=
NM_001012331.1:c.2049G>A , LRG_261t2:c.2049G>A NP_001012331.1:p.Leu683=
NM_002529.3:c.2067G>A , LRG_261t3:c.2067G>A NP_002520.2:p.Leu689=
NM_001012331.2:c.2049G>A NP_001012331.1:p.Leu683=
NM_002529.4:c.2067G>A MANE Select NP_002520.2:p.Leu689=