Canonical Allele Identifier: CA1168915

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156864766A>G , CM000663.2:g.156864766A>G	GRCh38
NC_000001.10:g.156834558A>G , CM000663.1:g.156834558A>G	GRCh37
NC_000001.9:g.155101182A>G	NCBI36
NG_007493.1:g.54017A>G , LRG_261:g.54017A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.326A>G MANE Select	NP_002520.2:p.Asp109Gly
ENST00000524377.7:c.326A>G MANE Select	ENSP00000431418.1:p.Asp109Gly
NM_001007792.1:c.236A>G , LRG_261t1:c.236A>G	NP_001007793.1:p.Asp79Gly
NM_001012331.1:c.326A>G , LRG_261t2:c.326A>G	NP_001012331.1:p.Asp109Gly
NM_001012331.2:c.326A>G	NP_001012331.1:p.Asp109Gly
NM_002529.3:c.326A>G , LRG_261t3:c.326A>G	NP_002520.2:p.Asp109Gly
ENST00000358660.3:c.326A>G	ENSP00000351486.3:p.Asp109Gly
ENST00000368196.7:c.326A>G	ENSP00000357179.3:p.Asp109Gly
ENST00000392302.6:c.236A>G	ENSP00000376120.2:p.Asp79Gly
ENST00000392302.7:c.164A>G	ENSP00000376120.3:p.Asp55Gly
ENST00000489021.6:n.313-8867A>G
ENST00000497019.6:c.236A>G	ENSP00000436804.1:p.Asp79Gly
ENST00000497019.7:c.164A>G	ENSP00000436804.2:p.Asp55Gly
ENST00000524377.5:c.326A>G	ENSP00000431418.1:p.Asp109Gly
ENST00000530298.5:n.384A>G
ENST00000533630.1:n.348A>G
ENST00000674537.1:c.164A>G	ENSP00000502725.1:p.Asp55Gly
ENST00000674537.2:c.164A>G	ENSP00000502725.1:p.Asp55Gly
ENST00000675461.1:c.326A>G	ENSP00000501668.1:p.Asp109Gly