Canonical Allele Identifier: CA342938096

Gene: NTRK1

Linked Data

• dbSNP Id: rs774290556
• MyVariant Identifiers: chr1:g.156845955T>A (hg19) ; chr1:g.156876163T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876163T>A , CM000663.2:g.156876163T>A	GRCh38
NC_000001.10:g.156845955T>A , CM000663.1:g.156845955T>A	GRCh37
NC_000001.9:g.155112579T>A	NCBI36
NG_007493.1:g.65414T>A , LRG_261:g.65414T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1405T>A	ENSP00000502725.1:p.Cys469Ser
ENST00000392302.7:c.1405T>A	ENSP00000376120.3:p.Cys469Ser
ENST00000497019.7:c.*177T>A	ENSP00000436804.2:n.*177T>A
ENST00000524377.7:c.1585T>A MANE Select	ENSP00000431418.1:p.Cys529Ser
ENST00000674537.1:c.1405T>A	ENSP00000502725.1:p.Cys469Ser
ENST00000358660.3:c.1576T>A	ENSP00000351486.3:p.Cys526Ser
ENST00000368196.7:c.1567T>A	ENSP00000357179.3:p.Cys523Ser
ENST00000392302.6:c.1477T>A	ENSP00000376120.2:p.Cys493Ser
ENST00000497019.6:c.*177T>A	ENSP00000436804.1:n.*177T>A
ENST00000524377.5:c.1585T>A	ENSP00000431418.1:p.Cys529Ser
ENST00000530298.5:n.2038T>A
ENST00000534682.1:n.808T>A
NM_001007792.1:c.1477T>A , LRG_261t1:c.1477T>A	NP_001007793.1:p.Cys493Ser
NM_001012331.1:c.1567T>A , LRG_261t2:c.1567T>A	NP_001012331.1:p.Cys523Ser
NM_002529.3:c.1585T>A , LRG_261t3:c.1585T>A	NP_002520.2:p.Cys529Ser
NM_001012331.2:c.1567T>A	NP_001012331.1:p.Cys523Ser
NM_002529.4:c.1585T>A MANE Select	NP_002520.2:p.Cys529Ser