Canonical Allele Identifier: CA421140614

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156851287G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881495G>T , CM000663.2:g.156881495G>T	GRCh38
NC_000001.10:g.156851287G>T , CM000663.1:g.156851287G>T	GRCh37
NC_000001.9:g.155117911G>T	NCBI36
NG_007493.1:g.70746G>T , LRG_261:g.70746G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.2064G>T	ENSP00000502725.1:p.Arg688=
ENST00000392302.7:c.2064G>T	ENSP00000376120.3:p.Arg688=
ENST00000497019.7:c.*836G>T	ENSP00000436804.2:n.*836G>T
ENST00000524377.7:c.2244G>T MANE Select	ENSP00000431418.1:p.Arg748=
ENST00000531606.2:c.303G>T
ENST00000674537.1:c.2064G>T	ENSP00000502725.1:p.Arg688=
ENST00000358660.3:c.2235G>T	ENSP00000351486.3:p.Arg745=
ENST00000368196.7:c.2226G>T	ENSP00000357179.3:p.Arg742=
ENST00000392302.6:c.2136G>T	ENSP00000376120.2:p.Arg712=
ENST00000497019.6:c.*836G>T	ENSP00000436804.1:n.*836G>T
ENST00000524377.5:c.2244G>T	ENSP00000431418.1:p.Arg748=
ENST00000530298.5:n.2697G>T
ENST00000531606.1:n.287G>T
NM_001007792.1:c.2136G>T , LRG_261t1:c.2136G>T	NP_001007793.1:p.Arg712=
NM_001012331.1:c.2226G>T , LRG_261t2:c.2226G>T	NP_001012331.1:p.Arg742=
NM_002529.3:c.2244G>T , LRG_261t3:c.2244G>T	NP_002520.2:p.Arg748=
NM_001012331.2:c.2226G>T	NP_001012331.1:p.Arg742=
NM_002529.4:c.2244G>T MANE Select	NP_002520.2:p.Arg748=