Canonical Allele Identifier: CA421140663

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102931264
• MyVariant Identifiers: chr1:g.156851365C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881573C>T , CM000663.2:g.156881573C>T	GRCh38
NC_000001.10:g.156851365C>T , CM000663.1:g.156851365C>T	GRCh37
NC_000001.9:g.155117989C>T	NCBI36
NG_007493.1:g.70824C>T , LRG_261:g.70824C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2142C>T	ENSP00000502725.1:p.Ile714=
ENST00000392302.7:c.2142C>T	ENSP00000376120.3:p.Ile714=
ENST00000497019.7:c.*914C>T	ENSP00000436804.2:n.*914C>T
ENST00000524377.7:c.2322C>T MANE Select	ENSP00000431418.1:p.Ile774=
ENST00000531606.2:c.381C>T
ENST00000674537.1:c.2142C>T	ENSP00000502725.1:p.Ile714=
ENST00000358660.3:c.2313C>T	ENSP00000351486.3:p.Ile771=
ENST00000368196.7:c.2304C>T	ENSP00000357179.3:p.Ile768=
ENST00000392302.6:c.2214C>T	ENSP00000376120.2:p.Ile738=
ENST00000497019.6:c.*914C>T	ENSP00000436804.1:n.*914C>T
ENST00000524377.5:c.2322C>T	ENSP00000431418.1:p.Ile774=
ENST00000530298.5:n.2775C>T
ENST00000531606.1:n.365C>T
NM_001007792.1:c.2214C>T , LRG_261t1:c.2214C>T	NP_001007793.1:p.Ile738=
NM_001012331.1:c.2304C>T , LRG_261t2:c.2304C>T	NP_001012331.1:p.Ile768=
NM_002529.3:c.2322C>T , LRG_261t3:c.2322C>T	NP_002520.2:p.Ile774=
NM_001012331.2:c.2304C>T	NP_001012331.1:p.Ile768=
NM_002529.4:c.2322C>T MANE Select	NP_002520.2:p.Ile774=