Canonical Allele Identifier: CA916080239

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 841216
• ClinVar RCV Id: RCV001043393

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156865026_156868108del , CM000663.2:g.156865026_156868108del	GRCh38
NC_000001.10:g.156834818_156837900del , CM000663.1:g.156834818_156837900del	GRCh37
NC_000001.9:g.155101442_155104524del	NCBI36
NG_007493.1:g.54277_57359del , LRG_261:g.54277_57359del

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.197+227_271del
ENST00000392302.7:c.197+227_271del
ENST00000497019.7:c.197+227_271del
ENST00000524377.7:c.359+227_433del
ENST00000674537.1:c.197+227_271del
ENST00000358660.3:c.359+227_433del
ENST00000368196.7:c.359+227_433del
ENST00000392302.6:c.269+227_343del
ENST00000489021.6:n.313-8607_313-5525del
ENST00000497019.6:c.269+227_343del
ENST00000524377.5:c.359+227_433del
ENST00000530298.5:n.417+227_491del
NM_001007792.1:c.269+227_343del , LRG_261t1:c.269+227_343del
NM_001012331.1:c.359+227_433del , LRG_261t2:c.359+227_433del
NM_002529.3:c.359+227_433del , LRG_261t3:c.359+227_433del
NM_001012331.2:c.359+227_433del
NM_002529.4:c.359+227_433del