Canonical Allele Identifier: CA889795474

Gene: NTRK1

Linked Data

• dbSNP Id: rs1207298666
• gnomAD v4: 1-156860740-A-AGGG
• MyVariant Identifiers: chr1:g.156830532_156830533insGGG (hg19) ; chr1:g.156860740_156860741insGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156860746_156860748dup , CM000663.2:g.156860746_156860748dup	GRCh38
NC_000001.10:g.156830538_156830540dup , CM000663.1:g.156830538_156830540dup	GRCh37
NC_000001.9:g.155097162_155097164dup	NCBI36
NG_007493.1:g.49997_49999dup , LRG_261:g.49997_49999dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.51-3608_51-3606dup	ENSP00000502725.1:n.51-3608_51-3606dup
ENST00000392302.7:c.51-3608_51-3606dup	ENSP00000376120.3:n.51-3608_51-3606dup
ENST00000497019.7:c.51-3608_51-3606dup	ENSP00000436804.2:n.51-3608_51-3606dup
ENST00000674537.1:c.51-3608_51-3606dup	ENSP00000502725.1:n.51-3608_51-3606dup
ENST00000392302.6:c.123-3608_123-3606dup	ENSP00000376120.2:n.123-3608_123-3606dup
ENST00000489021.6:n.313-12887_313-12885dup
ENST00000497019.6:c.123-3608_123-3606dup	ENSP00000436804.1:n.123-3608_123-3606dup
ENST00000530298.5:n.271-3608_271-3606dup
NM_001007792.1:c.123-3608_123-3606dup , LRG_261t1:c.123-3608_123-3606dup	NP_001007793.1:n.123-3608_123-3606dup