Canonical Allele Identifier: CA342936137

Gene: NTRK1

Linked Data

• dbSNP Id: rs121964869
• MyVariant Identifiers: chr1:g.156843650A>T (hg19) ; chr1:g.156873858A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156873858A>T , CM000663.2:g.156873858A>T	GRCh38
NC_000001.10:g.156843650A>T , CM000663.1:g.156843650A>T	GRCh37
NC_000001.9:g.155110274A>T	NCBI36
NG_007493.1:g.63109A>T , LRG_261:g.63109A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.914A>T	ENSP00000502725.1:p.Tyr305Phe
ENST00000392302.7:c.914A>T	ENSP00000376120.3:p.Tyr305Phe
ENST00000497019.7:c.781A>T	ENSP00000436804.2:p.Thr261Ser
ENST00000524377.7:c.1076A>T MANE Select	ENSP00000431418.1:p.Tyr359Phe
ENST00000674537.1:c.914A>T	ENSP00000502725.1:p.Tyr305Phe
ENST00000358660.3:c.1076A>T	ENSP00000351486.3:p.Tyr359Phe
ENST00000368196.7:c.1076A>T	ENSP00000357179.3:p.Tyr359Phe
ENST00000392302.6:c.986A>T	ENSP00000376120.2:p.Tyr329Phe
ENST00000489021.6:n.538A>T
ENST00000497019.6:c.853A>T	ENSP00000436804.1:p.Thr285Ser
ENST00000524377.5:c.1076A>T	ENSP00000431418.1:p.Tyr359Phe
ENST00000530298.5:n.1134A>T
NM_001007792.1:c.986A>T , LRG_261t1:c.986A>T	NP_001007793.1:p.Tyr329Phe
NM_001012331.1:c.1076A>T , LRG_261t2:c.1076A>T	NP_001012331.1:p.Tyr359Phe
NM_002529.3:c.1076A>T , LRG_261t3:c.1076A>T	NP_002520.2:p.Tyr359Phe
NM_001012331.2:c.1076A>T	NP_001012331.1:p.Tyr359Phe
NM_002529.4:c.1076A>T MANE Select	NP_002520.2:p.Tyr359Phe