Canonical Allele Identifier: CA526500422

Gene: NTRK1

Linked Data

• dbSNP Id: rs1309558720
• gnomAD v2: 1-156846043-AC-A
• gnomAD v4: 1-156876251-AC-A
• MyVariant Identifiers: chr1:g.156846044del (hg19) ; chr1:g.156876252del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876256del , CM000663.2:g.156876256del	GRCh38
NC_000001.10:g.156846048del , CM000663.1:g.156846048del	GRCh37
NC_000001.9:g.155112672del	NCBI36
NG_007493.1:g.65507del , LRG_261:g.65507del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1452+46del	ENSP00000502725.1:n.1452+46del
ENST00000392302.7:c.1452+46del	ENSP00000376120.3:n.1452+46del
ENST00000497019.7:c.*224+46del	ENSP00000436804.2:n.*224+46del
ENST00000524377.7:c.1632+46del MANE Select	ENSP00000431418.1:n.1632+46del
ENST00000674537.1:c.1452+46del	ENSP00000502725.1:n.1452+46del
ENST00000358660.3:c.1623+46del	ENSP00000351486.3:n.1623+46del
ENST00000368196.7:c.1614+46del	ENSP00000357179.3:n.1614+46del
ENST00000392302.6:c.1524+46del	ENSP00000376120.2:n.1524+46del
ENST00000497019.6:c.*224+46del	ENSP00000436804.1:n.*224+46del
ENST00000524377.5:c.1632+46del	ENSP00000431418.1:n.1632+46del
ENST00000530298.5:n.2085+46del
NM_001007792.1:c.1524+46del , LRG_261t1:c.1524+46del	NP_001007793.1:n.1524+46del
NM_001012331.1:c.1614+46del , LRG_261t2:c.1614+46del	NP_001012331.1:n.1614+46del
NM_002529.3:c.1632+46del , LRG_261t3:c.1632+46del	NP_002520.2:n.1632+46del
NM_001012331.2:c.1614+46del	NP_001012331.1:n.1614+46del
NM_002529.4:c.1632+46del MANE Select	NP_002520.2:n.1632+46del