Canonical Allele Identifier: CA342938051

Gene: NTRK1

Linked Data

• dbSNP Id: rs1351290687
• gnomAD v3: 1-156876151-T-G
• gnomAD v4: 1-156876151-T-G
• MyVariant Identifiers: chr1:g.156845943T>G (hg19) ; chr1:g.156876151T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876151T>G , CM000663.2:g.156876151T>G	GRCh38
NC_000001.10:g.156845943T>G , CM000663.1:g.156845943T>G	GRCh37
NC_000001.9:g.155112567T>G	NCBI36
NG_007493.1:g.65402T>G , LRG_261:g.65402T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1393T>G	ENSP00000502725.1:p.Phe465Val
ENST00000392302.7:c.1393T>G	ENSP00000376120.3:p.Phe465Val
ENST00000497019.7:c.*165T>G	ENSP00000436804.2:n.*165T>G
ENST00000524377.7:c.1573T>G MANE Select	ENSP00000431418.1:p.Phe525Val
ENST00000674537.1:c.1393T>G	ENSP00000502725.1:p.Phe465Val
ENST00000358660.3:c.1564T>G	ENSP00000351486.3:p.Phe522Val
ENST00000368196.7:c.1555T>G	ENSP00000357179.3:p.Phe519Val
ENST00000392302.6:c.1465T>G	ENSP00000376120.2:p.Phe489Val
ENST00000497019.6:c.*165T>G	ENSP00000436804.1:n.*165T>G
ENST00000524377.5:c.1573T>G	ENSP00000431418.1:p.Phe525Val
ENST00000530298.5:n.2026T>G
ENST00000534682.1:n.796T>G
NM_001007792.1:c.1465T>G , LRG_261t1:c.1465T>G	NP_001007793.1:p.Phe489Val
NM_001012331.1:c.1555T>G , LRG_261t2:c.1555T>G	NP_001012331.1:p.Phe519Val
NM_002529.3:c.1573T>G , LRG_261t3:c.1573T>G	NP_002520.2:p.Phe525Val
NM_001012331.2:c.1555T>G	NP_001012331.1:p.Phe519Val
NM_002529.4:c.1573T>G MANE Select	NP_002520.2:p.Phe525Val