Canonical Allele Identifier: CA2697494444

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102923896

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156879092G>A , CM000663.2:g.156879092G>A	GRCh38
NC_000001.10:g.156848884G>A , CM000663.1:g.156848884G>A	GRCh37
NC_000001.9:g.155115508G>A	NCBI36
NG_007493.1:g.68343G>A , LRG_261:g.68343G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1626-30G>A	ENSP00000502725.1:n.1626-30G>A
ENST00000392302.7:c.1626-30G>A	ENSP00000376120.3:n.1626-30G>A
ENST00000497019.7:c.*398-30G>A	ENSP00000436804.2:n.*398-30G>A
ENST00000524377.7:c.1806-30G>A MANE Select	ENSP00000431418.1:n.1806-30G>A
ENST00000674537.1:c.1626-30G>A	ENSP00000502725.1:n.1626-30G>A
ENST00000358660.3:c.1797-30G>A	ENSP00000351486.3:n.1797-30G>A
ENST00000368196.7:c.1788-30G>A	ENSP00000357179.3:n.1788-30G>A
ENST00000392302.6:c.1698-30G>A	ENSP00000376120.2:n.1698-30G>A
ENST00000497019.6:c.*398-30G>A	ENSP00000436804.1:n.*398-30G>A
ENST00000524377.5:c.1806-30G>A	ENSP00000431418.1:n.1806-30G>A
ENST00000530298.5:n.2259-30G>A
NM_001007792.1:c.1698-30G>A , LRG_261t1:c.1698-30G>A	NP_001007793.1:n.1698-30G>A
NM_001012331.1:c.1788-30G>A , LRG_261t2:c.1788-30G>A	NP_001012331.1:n.1788-30G>A
NM_002529.3:c.1806-30G>A , LRG_261t3:c.1806-30G>A	NP_002520.2:n.1806-30G>A
NM_001012331.2:c.1788-30G>A	NP_001012331.1:n.1788-30G>A
NM_002529.4:c.1806-30G>A MANE Select	NP_002520.2:n.1806-30G>A