Canonical Allele Identifier: CA342937490

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875610A>G , CM000663.2:g.156875610A>G	GRCh38
NC_000001.10:g.156845402A>G , CM000663.1:g.156845402A>G	GRCh37
NC_000001.9:g.155112026A>G	NCBI36
NG_007493.1:g.64861A>G , LRG_261:g.64861A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.1445A>G MANE Select	NP_002520.2:p.Lys482Arg
ENST00000524377.7:c.1445A>G MANE Select	ENSP00000431418.1:p.Lys482Arg
NM_001007792.1:c.1337A>G , LRG_261t1:c.1337A>G	NP_001007793.1:p.Lys446Arg
NM_001012331.1:c.1427A>G , LRG_261t2:c.1427A>G	NP_001012331.1:p.Lys476Arg
NM_001012331.2:c.1427A>G	NP_001012331.1:p.Lys476Arg
NM_002529.3:c.1445A>G , LRG_261t3:c.1445A>G	NP_002520.2:p.Lys482Arg
ENST00000358660.3:c.1427A>G	ENSP00000351486.3:p.Lys476Arg
ENST00000368196.7:c.1427A>G	ENSP00000357179.3:p.Lys476Arg
ENST00000392302.6:c.1337A>G	ENSP00000376120.2:p.Lys446Arg
ENST00000392302.7:c.1265A>G	ENSP00000376120.3:p.Lys422Arg
ENST00000497019.6:c.*37A>G	ENSP00000436804.1:n.*37A>G
ENST00000497019.7:c.*37A>G	ENSP00000436804.2:n.*37A>G
ENST00000524377.5:c.1445A>G	ENSP00000431418.1:p.Lys482Arg
ENST00000530298.5:n.1485A>G
ENST00000534682.1:n.668A>G
ENST00000674537.1:c.1265A>G	ENSP00000502725.1:p.Lys422Arg
ENST00000674537.2:c.1265A>G	ENSP00000502725.1:p.Lys422Arg