Canonical Allele Identifier: CA421270914

Gene: NTRK1

Linked Data

• MyVariant Identifiers: chr1:g.156837926T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156868134T>G , CM000663.2:g.156868134T>G	GRCh38
NC_000001.10:g.156837926T>G , CM000663.1:g.156837926T>G	GRCh37
NC_000001.9:g.155104550T>G	NCBI36
NG_007493.1:g.57385T>G , LRG_261:g.57385T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.297T>G	ENSP00000502725.1:p.Ser99=
ENST00000392302.7:c.297T>G	ENSP00000376120.3:p.Ser99=
ENST00000497019.7:c.297T>G	ENSP00000436804.2:p.Ser99=
ENST00000524377.7:c.459T>G MANE Select	ENSP00000431418.1:p.Ser153=
ENST00000674537.1:c.297T>G	ENSP00000502725.1:p.Ser99=
ENST00000358660.3:c.459T>G	ENSP00000351486.3:p.Ser153=
ENST00000368196.7:c.459T>G	ENSP00000357179.3:p.Ser153=
ENST00000392302.6:c.369T>G	ENSP00000376120.2:p.Ser123=
ENST00000489021.6:n.313-5499T>G
ENST00000497019.6:c.369T>G	ENSP00000436804.1:p.Ser123=
ENST00000524377.5:c.459T>G	ENSP00000431418.1:p.Ser153=
ENST00000530298.5:n.517T>G
NM_001007792.1:c.369T>G , LRG_261t1:c.369T>G	NP_001007793.1:p.Ser123=
NM_001012331.1:c.459T>G , LRG_261t2:c.459T>G	NP_001012331.1:p.Ser153=
NM_002529.3:c.459T>G , LRG_261t3:c.459T>G	NP_002520.2:p.Ser153=
NM_001012331.2:c.459T>G	NP_001012331.1:p.Ser153=
NM_002529.4:c.459T>G MANE Select	NP_002520.2:p.Ser153=