Canonical Allele Identifier: CA342938019

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102917499
• MyVariant Identifiers: chr1:g.156845937A>G (hg19) ; chr1:g.156876145A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876145A>G , CM000663.2:g.156876145A>G	GRCh38
NC_000001.10:g.156845937A>G , CM000663.1:g.156845937A>G	GRCh37
NC_000001.9:g.155112561A>G	NCBI36
NG_007493.1:g.65396A>G , LRG_261:g.65396A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1387A>G	ENSP00000502725.1:p.Lys463Glu
ENST00000392302.7:c.1387A>G	ENSP00000376120.3:p.Lys463Glu
ENST00000497019.7:c.*159A>G	ENSP00000436804.2:n.*159A>G
ENST00000524377.7:c.1567A>G MANE Select	ENSP00000431418.1:p.Lys523Glu
ENST00000674537.1:c.1387A>G	ENSP00000502725.1:p.Lys463Glu
ENST00000358660.3:c.1558A>G	ENSP00000351486.3:p.Lys520Glu
ENST00000368196.7:c.1549A>G	ENSP00000357179.3:p.Lys517Glu
ENST00000392302.6:c.1459A>G	ENSP00000376120.2:p.Lys487Glu
ENST00000497019.6:c.*159A>G	ENSP00000436804.1:n.*159A>G
ENST00000524377.5:c.1567A>G	ENSP00000431418.1:p.Lys523Glu
ENST00000530298.5:n.2020A>G
ENST00000534682.1:n.790A>G
NM_001007792.1:c.1459A>G , LRG_261t1:c.1459A>G	NP_001007793.1:p.Lys487Glu
NM_001012331.1:c.1549A>G , LRG_261t2:c.1549A>G	NP_001012331.1:p.Lys517Glu
NM_002529.3:c.1567A>G , LRG_261t3:c.1567A>G	NP_002520.2:p.Lys523Glu
NM_001012331.2:c.1549A>G	NP_001012331.1:p.Lys517Glu
NM_002529.4:c.1567A>G MANE Select	NP_002520.2:p.Lys523Glu