Canonical Allele Identifier: CA342937199

Gene: NTRK1

Linked Data

• dbSNP Id: rs202108805
• MyVariant Identifiers: chr1:g.156845315C>G (hg19) ; chr1:g.156875523C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875523C>G , CM000663.2:g.156875523C>G	GRCh38
NC_000001.10:g.156845315C>G , CM000663.1:g.156845315C>G	GRCh37
NC_000001.9:g.155111939C>G	NCBI36
NG_007493.1:g.64774C>G , LRG_261:g.64774C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1178C>G	ENSP00000502725.1:p.Pro393Arg
ENST00000392302.7:c.1178C>G	ENSP00000376120.3:p.Pro393Arg
ENST00000497019.7:c.1045C>G	ENSP00000436804.2:p.Arg349Gly
ENST00000524377.7:c.1358C>G MANE Select	ENSP00000431418.1:p.Pro453Arg
ENST00000674537.1:c.1178C>G	ENSP00000502725.1:p.Pro393Arg
ENST00000358660.3:c.1340C>G	ENSP00000351486.3:p.Pro447Arg
ENST00000368196.7:c.1340C>G	ENSP00000357179.3:p.Pro447Arg
ENST00000392302.6:c.1250C>G	ENSP00000376120.2:p.Pro417Arg
ENST00000497019.6:c.1117C>G	ENSP00000436804.1:p.Arg373Gly
ENST00000524377.5:c.1358C>G	ENSP00000431418.1:p.Pro453Arg
ENST00000530298.5:n.1398C>G
ENST00000534682.1:n.581C>G
NM_001007792.1:c.1250C>G , LRG_261t1:c.1250C>G	NP_001007793.1:p.Pro417Arg
NM_001012331.1:c.1340C>G , LRG_261t2:c.1340C>G	NP_001012331.1:p.Pro447Arg
NM_002529.3:c.1358C>G , LRG_261t3:c.1358C>G	NP_002520.2:p.Pro453Arg
NM_001012331.2:c.1340C>G	NP_001012331.1:p.Pro447Arg
NM_002529.4:c.1358C>G MANE Select	NP_002520.2:p.Pro453Arg