Canonical Allele Identifier: CA1169283

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875008C>T , CM000663.2:g.156875008C>T	GRCh38
NC_000001.10:g.156844800C>T , CM000663.1:g.156844800C>T	GRCh37
NC_000001.9:g.155111424C>T	NCBI36
NG_007493.1:g.64259C>T , LRG_261:g.64259C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1174C>T	ENSP00000502725.1:p.Arg392Cys
ENST00000392302.7:c.1174C>T	ENSP00000376120.3:p.Arg392Cys
ENST00000497019.7:c.1041C>T	ENSP00000436804.2:p.Thr347=
ENST00000524377.7:c.1354C>T MANE Select	ENSP00000431418.1:p.Arg452Cys
ENST00000674537.1:c.1174C>T	ENSP00000502725.1:p.Arg392Cys
ENST00000358660.3:c.1336C>T	ENSP00000351486.3:p.Arg446Cys
ENST00000368196.7:c.1336C>T	ENSP00000357179.3:p.Arg446Cys
ENST00000392302.6:c.1246C>T	ENSP00000376120.2:p.Arg416Cys
ENST00000497019.6:c.1113C>T	ENSP00000436804.1:p.Thr371=
ENST00000524377.5:c.1354C>T	ENSP00000431418.1:p.Arg452Cys
ENST00000530298.5:n.1394C>T
ENST00000534682.1:n.577C>T
NM_001007792.1:c.1246C>T , LRG_261t1:c.1246C>T	NP_001007793.1:p.Arg416Cys
NM_001012331.1:c.1336C>T , LRG_261t2:c.1336C>T	NP_001012331.1:p.Arg446Cys
NM_002529.3:c.1354C>T , LRG_261t3:c.1354C>T	NP_002520.2:p.Arg452Cys
NM_001012331.2:c.1336C>T	NP_001012331.1:p.Arg446Cys
NM_002529.4:c.1354C>T MANE Select	NP_002520.2:p.Arg452Cys