Canonical Allele Identifier: CA645518200

Gene: NTRK1

Linked Data

• COSMIC: COSM6058580 ; COSM6058581

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876437_156876438delinsAT , CM000663.2:g.156876437_156876438delinsAT	GRCh38
NC_000001.10:g.156846229_156846230delinsAT , CM000663.1:g.156846229_156846230delinsAT	GRCh37
NC_000001.9:g.155112853_155112854delinsAT	NCBI36
NG_007493.1:g.65688_65689delinsAT , LRG_261:g.65688_65689delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1490_1491delinsAT	ENSP00000502725.1:p.Phe497Tyr
ENST00000392302.7:c.1490_1491delinsAT	ENSP00000376120.3:p.Phe497Tyr
ENST00000497019.7:c.*262_*263delinsAT	ENSP00000436804.2:n.*262_*263delinsAT
ENST00000524377.7:c.1670_1671delinsAT MANE Select	ENSP00000431418.1:p.Phe557Tyr
ENST00000674537.1:c.1490_1491delinsAT	ENSP00000502725.1:p.Phe497Tyr
ENST00000358660.3:c.1661_1662delinsAT	ENSP00000351486.3:p.Phe554Tyr
ENST00000368196.7:c.1652_1653delinsAT	ENSP00000357179.3:p.Phe551Tyr
ENST00000392302.6:c.1562_1563delinsAT	ENSP00000376120.2:p.Phe521Tyr
ENST00000497019.6:c.*262_*263delinsAT	ENSP00000436804.1:n.*262_*263delinsAT
ENST00000524377.5:c.1670_1671delinsAT	ENSP00000431418.1:p.Phe557Tyr
ENST00000530298.5:n.2123_2124delinsAT
NM_001007792.1:c.1562_1563delinsAT , LRG_261t1:c.1562_1563delinsAT	NP_001007793.1:p.Phe521Tyr
NM_001012331.1:c.1652_1653delinsAT , LRG_261t2:c.1652_1653delinsAT	NP_001012331.1:p.Phe551Tyr
NM_002529.3:c.1670_1671delinsAT , LRG_261t3:c.1670_1671delinsAT	NP_002520.2:p.Phe557Tyr
NM_001012331.2:c.1652_1653delinsAT	NP_001012331.1:p.Phe551Tyr
NM_002529.4:c.1670_1671delinsAT MANE Select	NP_002520.2:p.Phe557Tyr