Canonical Allele Identifier: CA2838905556

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876494dup , CM000663.2:g.156876494dup	GRCh38
NC_000001.10:g.156846286dup , CM000663.1:g.156846286dup	GRCh37
NC_000001.9:g.155112910dup	NCBI36
NG_007493.1:g.65745dup , LRG_261:g.65745dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1547dup	ENSP00000502725.1:p.Gly517ArgfsTer14
ENST00000392302.7:c.1547dup	ENSP00000376120.3:p.Gly517ArgfsTer14
ENST00000497019.7:c.*319dup	ENSP00000436804.2:n.*319dup
ENST00000524377.7:c.1727dup MANE Select	ENSP00000431418.1:p.Gly577ArgfsTer14
ENST00000674537.1:c.1547dup	ENSP00000502725.1:p.Gly517ArgfsTer14
ENST00000358660.3:c.1718dup	ENSP00000351486.3:p.Gly574ArgfsTer14
ENST00000368196.7:c.1709dup	ENSP00000357179.3:p.Gly571ArgfsTer14
ENST00000392302.6:c.1619dup	ENSP00000376120.2:p.Gly541ArgfsTer14
ENST00000497019.6:c.*319dup	ENSP00000436804.1:n.*319dup
ENST00000524377.5:c.1727dup	ENSP00000431418.1:p.Gly577ArgfsTer14
ENST00000530298.5:n.2180dup
NM_001007792.1:c.1619dup , LRG_261t1:c.1619dup	NP_001007793.1:p.Gly541ArgfsTer14
NM_001012331.1:c.1709dup , LRG_261t2:c.1709dup	NP_001012331.1:p.Gly571ArgfsTer14
NM_002529.3:c.1727dup , LRG_261t3:c.1727dup	NP_002520.2:p.Gly577ArgfsTer14
NM_001012331.2:c.1709dup	NP_001012331.1:p.Gly571ArgfsTer14
NM_002529.4:c.1727dup MANE Select	NP_002520.2:p.Gly577ArgfsTer14