Canonical Allele Identifier: CA1169274

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156874955C>T , CM000663.2:g.156874955C>T	GRCh38
NC_000001.10:g.156844747C>T , CM000663.1:g.156844747C>T	GRCh37
NC_000001.9:g.155111371C>T	NCBI36
NG_007493.1:g.64206C>T , LRG_261:g.64206C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.1301C>T MANE Select	NP_002520.2:p.Thr434Met
ENST00000524377.7:c.1301C>T MANE Select	ENSP00000431418.1:p.Thr434Met
NM_001007792.1:c.1193C>T , LRG_261t1:c.1193C>T	NP_001007793.1:p.Thr398Met
NM_001012331.1:c.1283C>T , LRG_261t2:c.1283C>T	NP_001012331.1:p.Thr428Met
NM_001012331.2:c.1283C>T	NP_001012331.1:p.Thr428Met
NM_002529.3:c.1301C>T , LRG_261t3:c.1301C>T	NP_002520.2:p.Thr434Met
ENST00000358660.3:c.1283C>T	ENSP00000351486.3:p.Thr428Met
ENST00000368196.7:c.1283C>T	ENSP00000357179.3:p.Thr428Met
ENST00000392302.6:c.1193C>T	ENSP00000376120.2:p.Thr398Met
ENST00000392302.7:c.1121C>T	ENSP00000376120.3:p.Thr374Met
ENST00000497019.6:c.1060C>T	ENSP00000436804.1:p.Arg354Cys
ENST00000497019.7:c.988C>T	ENSP00000436804.2:p.Arg330Cys
ENST00000524377.5:c.1301C>T	ENSP00000431418.1:p.Thr434Met
ENST00000530298.5:n.1341C>T
ENST00000534682.1:n.524C>T
ENST00000674537.1:c.1121C>T	ENSP00000502725.1:p.Thr374Met
ENST00000674537.2:c.1121C>T	ENSP00000502725.1:p.Thr374Met