Canonical Allele Identifier: CA1168904
Gene: NTRK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 456616
dbSNP Id: rs201509045

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156864735G>A , CM000663.2:g.156864735G>A GRCh38
NC_000001.10:g.156834527G>A , CM000663.1:g.156834527G>A GRCh37
NC_000001.9:g.155101151G>A NCBI36
NG_007493.1:g.53986G>A , LRG_261:g.53986G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392302.7:c.133G>A ENSP00000376120.3:p.Val45Met
ENST00000497019.7:c.133G>A ENSP00000436804.2:p.Val45Met
ENST00000524377.7:c.295G>A MANE Select ENSP00000431418.1:p.Val99Met
ENST00000674537.1:c.133G>A ENSP00000502725.1:p.Val45Met
ENST00000675461.1:n.295G>A ENSP00000501668.1:p.Val99Met
ENST00000358660.3:c.295G>A ENSP00000351486.3:p.Val99Met
ENST00000368196.7:c.295G>A ENSP00000357179.3:p.Val99Met
ENST00000392302.6:c.205G>A ENSP00000376120.2:p.Val69Met
ENST00000489021.6:n.313-8898G>A
ENST00000497019.6:c.205G>A ENSP00000436804.1:p.Val69Met
ENST00000524377.5:c.295G>A ENSP00000431418.1:p.Val99Met
ENST00000530298.5:n.353G>A
ENST00000533630.1:n.317G>A
NM_001007792.1:c.205G>A , LRG_261t1:c.205G>A NP_001007793.1:p.Val69Met
NM_001012331.1:c.295G>A , LRG_261t2:c.295G>A NP_001012331.1:p.Val99Met
NM_002529.3:c.295G>A , LRG_261t3:c.295G>A NP_002520.2:p.Val99Met
NM_001012331.2:c.295G>A NP_001012331.1:p.Val99Met
NM_002529.4:c.295G>A MANE Select NP_002520.2:p.Val99Met