Canonical Allele Identifier: CA342932572

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102886152
• MyVariant Identifiers: chr1:g.156834539C>G (hg19) ; chr1:g.156864747C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156864747C>G , CM000663.2:g.156864747C>G	GRCh38
NC_000001.10:g.156834539C>G , CM000663.1:g.156834539C>G	GRCh37
NC_000001.9:g.155101163C>G	NCBI36
NG_007493.1:g.53998C>G , LRG_261:g.53998C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.145C>G	ENSP00000502725.1:p.Leu49Val
ENST00000392302.7:c.145C>G	ENSP00000376120.3:p.Leu49Val
ENST00000497019.7:c.145C>G	ENSP00000436804.2:p.Leu49Val
ENST00000524377.7:c.307C>G MANE Select	ENSP00000431418.1:p.Leu103Val
ENST00000674537.1:c.145C>G	ENSP00000502725.1:p.Leu49Val
ENST00000675461.1:c.307C>G	ENSP00000501668.1:p.Leu103Val
ENST00000358660.3:c.307C>G	ENSP00000351486.3:p.Leu103Val
ENST00000368196.7:c.307C>G	ENSP00000357179.3:p.Leu103Val
ENST00000392302.6:c.217C>G	ENSP00000376120.2:p.Leu73Val
ENST00000489021.6:n.313-8886C>G
ENST00000497019.6:c.217C>G	ENSP00000436804.1:p.Leu73Val
ENST00000524377.5:c.307C>G	ENSP00000431418.1:p.Leu103Val
ENST00000530298.5:n.365C>G
ENST00000533630.1:n.329C>G
NM_001007792.1:c.217C>G , LRG_261t1:c.217C>G	NP_001007793.1:p.Leu73Val
NM_001012331.1:c.307C>G , LRG_261t2:c.307C>G	NP_001012331.1:p.Leu103Val
NM_002529.3:c.307C>G , LRG_261t3:c.307C>G	NP_002520.2:p.Leu103Val
NM_001012331.2:c.307C>G	NP_001012331.1:p.Leu103Val
NM_002529.4:c.307C>G MANE Select	NP_002520.2:p.Leu103Val