Canonical Allele Identifier: CA1169636

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881589C>T , CM000663.2:g.156881589C>T	GRCh38
NC_000001.10:g.156851381C>T , CM000663.1:g.156851381C>T	GRCh37
NC_000001.9:g.155118005C>T	NCBI36
NG_007493.1:g.70840C>T , LRG_261:g.70840C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.2338C>T MANE Select	NP_002520.2:p.Arg780Trp
ENST00000524377.7:c.2338C>T MANE Select	ENSP00000431418.1:p.Arg780Trp
NM_001007792.1:c.2230C>T , LRG_261t1:c.2230C>T	NP_001007793.1:p.Arg744Trp
NM_001012331.1:c.2320C>T , LRG_261t2:c.2320C>T	NP_001012331.1:p.Arg774Trp
NM_001012331.2:c.2320C>T	NP_001012331.1:p.Arg774Trp
NM_002529.3:c.2338C>T , LRG_261t3:c.2338C>T	NP_002520.2:p.Arg780Trp
ENST00000358660.3:c.2329C>T	ENSP00000351486.3:p.Arg777Trp
ENST00000368196.7:c.2320C>T	ENSP00000357179.3:p.Arg774Trp
ENST00000392302.6:c.2230C>T	ENSP00000376120.2:p.Arg744Trp
ENST00000392302.7:c.2158C>T	ENSP00000376120.3:p.Arg720Trp
ENST00000497019.6:c.*930C>T	ENSP00000436804.1:n.*930C>T
ENST00000497019.7:c.*930C>T	ENSP00000436804.2:n.*930C>T
ENST00000524377.5:c.2338C>T	ENSP00000431418.1:p.Arg780Trp
ENST00000530298.5:n.2791C>T
ENST00000531606.1:n.381C>T
ENST00000531606.2:c.397C>T
ENST00000674537.1:c.2158C>T	ENSP00000502725.1:p.Arg720Trp
ENST00000674537.2:c.2158C>T	ENSP00000502725.1:p.Arg720Trp