Canonical Allele Identifier: CA2648461499

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156864672-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156864672C>T , CM000663.2:g.156864672C>T	GRCh38
NC_000001.10:g.156834464C>T , CM000663.1:g.156834464C>T	GRCh37
NC_000001.9:g.155101088C>T	NCBI36
NG_007493.1:g.53923C>T , LRG_261:g.53923C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.126-56C>T	ENSP00000502725.1:n.126-56C>T
ENST00000392302.7:c.126-56C>T	ENSP00000376120.3:n.126-56C>T
ENST00000497019.7:c.126-56C>T	ENSP00000436804.2:n.126-56C>T
ENST00000524377.7:c.288-56C>T MANE Select	ENSP00000431418.1:n.288-56C>T
ENST00000674537.1:c.126-56C>T	ENSP00000502725.1:n.126-56C>T
ENST00000675461.1:c.288-56C>T	ENSP00000501668.1:n.288-56C>T
ENST00000358660.3:c.288-56C>T	ENSP00000351486.3:n.288-56C>T
ENST00000368196.7:c.288-56C>T	ENSP00000357179.3:n.288-56C>T
ENST00000392302.6:c.198-56C>T	ENSP00000376120.2:n.198-56C>T
ENST00000489021.6:n.313-8961C>T
ENST00000497019.6:c.198-56C>T	ENSP00000436804.1:n.198-56C>T
ENST00000524377.5:c.288-56C>T	ENSP00000431418.1:n.288-56C>T
ENST00000530298.5:n.346-56C>T
ENST00000533630.1:n.310-56C>T
NM_001007792.1:c.198-56C>T , LRG_261t1:c.198-56C>T	NP_001007793.1:n.198-56C>T
NM_001012331.1:c.288-56C>T , LRG_261t2:c.288-56C>T	NP_001012331.1:n.288-56C>T
NM_002529.3:c.288-56C>T , LRG_261t3:c.288-56C>T	NP_002520.2:n.288-56C>T
NM_001012331.2:c.288-56C>T	NP_001012331.1:n.288-56C>T
NM_002529.4:c.288-56C>T MANE Select	NP_002520.2:n.288-56C>T