Canonical Allele Identifier: CA342941471

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102930750
• MyVariant Identifiers: chr1:g.156851289C>G (hg19) ; chr1:g.156881497C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881497C>G , CM000663.2:g.156881497C>G	GRCh38
NC_000001.10:g.156851289C>G , CM000663.1:g.156851289C>G	GRCh37
NC_000001.9:g.155117913C>G	NCBI36
NG_007493.1:g.70748C>G , LRG_261:g.70748C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.2066C>G	ENSP00000502725.1:p.Pro689Arg
ENST00000392302.7:c.2066C>G	ENSP00000376120.3:p.Pro689Arg
ENST00000497019.7:c.*838C>G	ENSP00000436804.2:n.*838C>G
ENST00000524377.7:c.2246C>G MANE Select	ENSP00000431418.1:p.Pro749Arg
ENST00000531606.2:c.305C>G
ENST00000674537.1:c.2066C>G	ENSP00000502725.1:p.Pro689Arg
ENST00000358660.3:c.2237C>G	ENSP00000351486.3:p.Pro746Arg
ENST00000368196.7:c.2228C>G	ENSP00000357179.3:p.Pro743Arg
ENST00000392302.6:c.2138C>G	ENSP00000376120.2:p.Pro713Arg
ENST00000497019.6:c.*838C>G	ENSP00000436804.1:n.*838C>G
ENST00000524377.5:c.2246C>G	ENSP00000431418.1:p.Pro749Arg
ENST00000530298.5:n.2699C>G
ENST00000531606.1:n.289C>G
NM_001007792.1:c.2138C>G , LRG_261t1:c.2138C>G	NP_001007793.1:p.Pro713Arg
NM_001012331.1:c.2228C>G , LRG_261t2:c.2228C>G	NP_001012331.1:p.Pro743Arg
NM_002529.3:c.2246C>G , LRG_261t3:c.2246C>G	NP_002520.2:p.Pro749Arg
NM_001012331.2:c.2228C>G	NP_001012331.1:p.Pro743Arg
NM_002529.4:c.2246C>G MANE Select	NP_002520.2:p.Pro749Arg