Canonical Allele Identifier: CA2648465083

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156860861-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860865_156860866dup , CM000663.2:g.156860865_156860866dup	GRCh38
NC_000001.10:g.156830657_156830658dup , CM000663.1:g.156830657_156830658dup	GRCh37
NC_000001.9:g.155097281_155097282dup	NCBI36
NG_007493.1:g.50116_50117dup , LRG_261:g.50116_50117dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.51-3489_51-3488dup	ENSP00000502725.1:n.51-3489_51-3488dup
ENST00000392302.7:c.51-3489_51-3488dup	ENSP00000376120.3:n.51-3489_51-3488dup
ENST00000497019.7:c.51-3489_51-3488dup	ENSP00000436804.2:n.51-3489_51-3488dup
ENST00000674537.1:c.51-3489_51-3488dup	ENSP00000502725.1:n.51-3489_51-3488dup
ENST00000368196.7:c.-70_-69dup	ENSP00000357179.3:n.-70_-69dup
ENST00000392302.6:c.123-3489_123-3488dup	ENSP00000376120.2:n.123-3489_123-3488dup
ENST00000489021.6:n.313-12768_313-12767dup
ENST00000497019.6:c.123-3489_123-3488dup	ENSP00000436804.1:n.123-3489_123-3488dup
ENST00000530298.5:n.271-3489_271-3488dup
NM_001007792.1:c.123-3489_123-3488dup , LRG_261t1:c.123-3489_123-3488dup	NP_001007793.1:n.123-3489_123-3488dup