Canonical Allele Identifier: CA342936139

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156873859C>G , CM000663.2:g.156873859C>G	GRCh38
NC_000001.10:g.156843651C>G , CM000663.1:g.156843651C>G	GRCh37
NC_000001.9:g.155110275C>G	NCBI36
NG_007493.1:g.63110C>G , LRG_261:g.63110C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.1077C>G MANE Select	NP_002520.2:p.Tyr359Ter
ENST00000524377.7:c.1077C>G MANE Select	ENSP00000431418.1:p.Tyr359Ter
NM_001007792.1:c.987C>G , LRG_261t1:c.987C>G	NP_001007793.1:p.Tyr329Ter
NM_001012331.1:c.1077C>G , LRG_261t2:c.1077C>G	NP_001012331.1:p.Tyr359Ter
NM_001012331.2:c.1077C>G	NP_001012331.1:p.Tyr359Ter
NM_002529.3:c.1077C>G , LRG_261t3:c.1077C>G	NP_002520.2:p.Tyr359Ter
ENST00000358660.3:c.1077C>G	ENSP00000351486.3:p.Tyr359Ter
ENST00000368196.7:c.1077C>G	ENSP00000357179.3:p.Tyr359Ter
ENST00000392302.6:c.987C>G	ENSP00000376120.2:p.Tyr329Ter
ENST00000392302.7:c.915C>G	ENSP00000376120.3:p.Tyr305Ter
ENST00000489021.6:n.539C>G
ENST00000497019.6:c.854C>G	ENSP00000436804.1:p.Thr285Arg
ENST00000497019.7:c.782C>G	ENSP00000436804.2:p.Thr261Arg
ENST00000524377.5:c.1077C>G	ENSP00000431418.1:p.Tyr359Ter
ENST00000530298.5:n.1135C>G
ENST00000674537.1:c.915C>G	ENSP00000502725.1:p.Tyr305Ter
ENST00000674537.2:c.915C>G	ENSP00000502725.1:p.Tyr305Ter