Canonical Allele Identifier: CA1169279

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156874974C>G , CM000663.2:g.156874974C>G	GRCh38
NC_000001.10:g.156844766C>G , CM000663.1:g.156844766C>G	GRCh37
NC_000001.9:g.155111390C>G	NCBI36
NG_007493.1:g.64225C>G , LRG_261:g.64225C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1140C>G	ENSP00000502725.1:p.Asn380Lys
ENST00000392302.7:c.1140C>G	ENSP00000376120.3:p.Asn380Lys
ENST00000497019.7:c.1007C>G	ENSP00000436804.2:p.Thr336Arg
ENST00000524377.7:c.1320C>G MANE Select	ENSP00000431418.1:p.Asn440Lys
ENST00000674537.1:c.1140C>G	ENSP00000502725.1:p.Asn380Lys
ENST00000358660.3:c.1302C>G	ENSP00000351486.3:p.Asn434Lys
ENST00000368196.7:c.1302C>G	ENSP00000357179.3:p.Asn434Lys
ENST00000392302.6:c.1212C>G	ENSP00000376120.2:p.Asn404Lys
ENST00000497019.6:c.1079C>G	ENSP00000436804.1:p.Thr360Arg
ENST00000524377.5:c.1320C>G	ENSP00000431418.1:p.Asn440Lys
ENST00000530298.5:n.1360C>G
ENST00000534682.1:n.543C>G
NM_001007792.1:c.1212C>G , LRG_261t1:c.1212C>G	NP_001007793.1:p.Asn404Lys
NM_001012331.1:c.1302C>G , LRG_261t2:c.1302C>G	NP_001012331.1:p.Asn434Lys
NM_002529.3:c.1320C>G , LRG_261t3:c.1320C>G	NP_002520.2:p.Asn440Lys
NM_001012331.2:c.1302C>G	NP_001012331.1:p.Asn434Lys
NM_002529.4:c.1320C>G MANE Select	NP_002520.2:p.Asn440Lys