Canonical Allele Identifier: CA16617006
Gene: NTRK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 418391
ClinVar RCV Id: RCV000484442 RCV001828497
dbSNP Id: rs1064793219
MyVariant Identifiers: chr1:g.156838354T>A (hg19) chr1:g.156868562T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156868562T>A , CM000663.2:g.156868562T>A GRCh38
NC_000001.10:g.156838354T>A , CM000663.1:g.156838354T>A GRCh37
NC_000001.9:g.155104978T>A NCBI36
NG_007493.1:g.57813T>A , LRG_261:g.57813T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.470T>A ENSP00000502725.1:p.Val157Glu
ENST00000392302.7:c.470T>A ENSP00000376120.3:p.Val157Glu
ENST00000497019.7:c.470T>A ENSP00000436804.2:p.Val157Glu
ENST00000524377.7:c.632T>A MANE Select ENSP00000431418.1:p.Val211Glu
ENST00000674537.1:c.470T>A ENSP00000502725.1:p.Val157Glu
ENST00000358660.3:c.632T>A ENSP00000351486.3:p.Val211Glu
ENST00000368196.7:c.632T>A ENSP00000357179.3:p.Val211Glu
ENST00000392302.6:c.542T>A ENSP00000376120.2:p.Val181Glu
ENST00000489021.6:n.313-5071T>A
ENST00000497019.6:c.542T>A ENSP00000436804.1:p.Val181Glu
ENST00000524377.5:c.632T>A ENSP00000431418.1:p.Val211Glu
ENST00000530298.5:n.690T>A
NM_001007792.1:c.542T>A , LRG_261t1:c.542T>A NP_001007793.1:p.Val181Glu
NM_001012331.1:c.632T>A , LRG_261t2:c.632T>A NP_001012331.1:p.Val211Glu
NM_002529.3:c.632T>A , LRG_261t3:c.632T>A NP_002520.2:p.Val211Glu
NM_001012331.2:c.632T>A NP_001012331.1:p.Val211Glu
NM_002529.4:c.632T>A MANE Select NP_002520.2:p.Val211Glu
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Search 100 bp 3'