Canonical Allele Identifier: CA421137948

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102917204
• COSMIC: COSM283406 ; COSM283407
• MyVariant Identifiers: chr1:g.156845888G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876096G>A , CM000663.2:g.156876096G>A	GRCh38
NC_000001.10:g.156845888G>A , CM000663.1:g.156845888G>A	GRCh37
NC_000001.9:g.155112512G>A	NCBI36
NG_007493.1:g.65347G>A , LRG_261:g.65347G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1338G>A	ENSP00000502725.1:p.Lys446=
ENST00000392302.7:c.1338G>A	ENSP00000376120.3:p.Lys446=
ENST00000497019.7:c.*110G>A	ENSP00000436804.2:n.*110G>A
ENST00000524377.7:c.1518G>A MANE Select	ENSP00000431418.1:p.Lys506=
ENST00000674537.1:c.1338G>A	ENSP00000502725.1:p.Lys446=
ENST00000358660.3:c.1509G>A	ENSP00000351486.3:p.Lys503=
ENST00000368196.7:c.1500G>A	ENSP00000357179.3:p.Lys500=
ENST00000392302.6:c.1410G>A	ENSP00000376120.2:p.Lys470=
ENST00000497019.6:c.*110G>A	ENSP00000436804.1:n.*110G>A
ENST00000524377.5:c.1518G>A	ENSP00000431418.1:p.Lys506=
ENST00000530298.5:n.1971G>A
ENST00000534682.1:n.741G>A
NM_001007792.1:c.1410G>A , LRG_261t1:c.1410G>A	NP_001007793.1:p.Lys470=
NM_001012331.1:c.1500G>A , LRG_261t2:c.1500G>A	NP_001012331.1:p.Lys500=
NM_002529.3:c.1518G>A , LRG_261t3:c.1518G>A	NP_002520.2:p.Lys506=
NM_001012331.2:c.1500G>A	NP_001012331.1:p.Lys500=
NM_002529.4:c.1518G>A MANE Select	NP_002520.2:p.Lys506=