Canonical Allele Identifier: CA2648464890

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156860805-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860805_156860806insT , CM000663.2:g.156860805_156860806insT	GRCh38
NC_000001.10:g.156830597_156830598insT , CM000663.1:g.156830597_156830598insT	GRCh37
NC_000001.9:g.155097221_155097222insT	NCBI36
NG_007493.1:g.50056_50057insT , LRG_261:g.50056_50057insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.51-3549_51-3548insT	ENSP00000502725.1:n.51-3549_51-3548insT
ENST00000392302.7:c.51-3549_51-3548insT	ENSP00000376120.3:n.51-3549_51-3548insT
ENST00000497019.7:c.51-3549_51-3548insT	ENSP00000436804.2:n.51-3549_51-3548insT
ENST00000674537.1:c.51-3549_51-3548insT	ENSP00000502725.1:n.51-3549_51-3548insT
ENST00000392302.6:c.123-3549_123-3548insT	ENSP00000376120.2:n.123-3549_123-3548insT
ENST00000489021.6:n.313-12828_313-12827insT
ENST00000497019.6:c.123-3549_123-3548insT	ENSP00000436804.1:n.123-3549_123-3548insT
ENST00000530298.5:n.271-3549_271-3548insT
NM_001007792.1:c.123-3549_123-3548insT , LRG_261t1:c.123-3549_123-3548insT	NP_001007793.1:n.123-3549_123-3548insT