Canonical Allele Identifier: CA342937978

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102917435
• MyVariant Identifiers: chr1:g.156845926G>A (hg19) ; chr1:g.156876134G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876134G>A , CM000663.2:g.156876134G>A	GRCh38
NC_000001.10:g.156845926G>A , CM000663.1:g.156845926G>A	GRCh37
NC_000001.9:g.155112550G>A	NCBI36
NG_007493.1:g.65385G>A , LRG_261:g.65385G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1376G>A	ENSP00000502725.1:p.Gly459Asp
ENST00000392302.7:c.1376G>A	ENSP00000376120.3:p.Gly459Asp
ENST00000497019.7:c.*148G>A	ENSP00000436804.2:n.*148G>A
ENST00000524377.7:c.1556G>A MANE Select	ENSP00000431418.1:p.Gly519Asp
ENST00000674537.1:c.1376G>A	ENSP00000502725.1:p.Gly459Asp
ENST00000358660.3:c.1547G>A	ENSP00000351486.3:p.Gly516Asp
ENST00000368196.7:c.1538G>A	ENSP00000357179.3:p.Gly513Asp
ENST00000392302.6:c.1448G>A	ENSP00000376120.2:p.Gly483Asp
ENST00000497019.6:c.*148G>A	ENSP00000436804.1:n.*148G>A
ENST00000524377.5:c.1556G>A	ENSP00000431418.1:p.Gly519Asp
ENST00000530298.5:n.2009G>A
ENST00000534682.1:n.779G>A
NM_001007792.1:c.1448G>A , LRG_261t1:c.1448G>A	NP_001007793.1:p.Gly483Asp
NM_001012331.1:c.1538G>A , LRG_261t2:c.1538G>A	NP_001012331.1:p.Gly513Asp
NM_002529.3:c.1556G>A , LRG_261t3:c.1556G>A	NP_002520.2:p.Gly519Asp
NM_001012331.2:c.1538G>A	NP_001012331.1:p.Gly513Asp
NM_002529.4:c.1556G>A MANE Select	NP_002520.2:p.Gly519Asp