Canonical Allele Identifier: CA342936919

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156874941C>A , CM000663.2:g.156874941C>A	GRCh38
NC_000001.10:g.156844733C>A , CM000663.1:g.156844733C>A	GRCh37
NC_000001.9:g.155111357C>A	NCBI36
NG_007493.1:g.64192C>A , LRG_261:g.64192C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.1287C>A MANE Select	NP_002520.2:p.Cys429Ter
ENST00000524377.7:c.1287C>A MANE Select	ENSP00000431418.1:p.Cys429Ter
NM_001007792.1:c.1179C>A , LRG_261t1:c.1179C>A	NP_001007793.1:p.Cys393Ter
NM_001012331.1:c.1269C>A , LRG_261t2:c.1269C>A	NP_001012331.1:p.Cys423Ter
NM_001012331.2:c.1269C>A	NP_001012331.1:p.Cys423Ter
NM_002529.3:c.1287C>A , LRG_261t3:c.1287C>A	NP_002520.2:p.Cys429Ter
ENST00000358660.3:c.1269C>A	ENSP00000351486.3:p.Cys423Ter
ENST00000368196.7:c.1269C>A	ENSP00000357179.3:p.Cys423Ter
ENST00000392302.6:c.1179C>A	ENSP00000376120.2:p.Cys393Ter
ENST00000392302.7:c.1107C>A	ENSP00000376120.3:p.Cys369Ter
ENST00000497019.6:c.1046C>A	ENSP00000436804.1:p.Ala349Asp
ENST00000497019.7:c.974C>A	ENSP00000436804.2:p.Ala325Asp
ENST00000524377.5:c.1287C>A	ENSP00000431418.1:p.Cys429Ter
ENST00000530298.5:n.1327C>A
ENST00000534682.1:n.510C>A
ENST00000674537.1:c.1107C>A	ENSP00000502725.1:p.Cys369Ter
ENST00000674537.2:c.1107C>A	ENSP00000502725.1:p.Cys369Ter