Canonical Allele Identifier: CA421140652

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 989639
• ClinVar RCV Id: RCV001277510
• dbSNP Id: rs753397054
• gnomAD v4: 1-156881552-G-A
• MyVariant Identifiers: chr1:g.156851344G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156881552G>A , CM000663.2:g.156881552G>A	GRCh38
NC_000001.10:g.156851344G>A , CM000663.1:g.156851344G>A	GRCh37
NC_000001.9:g.155117968G>A	NCBI36
NG_007493.1:g.70803G>A , LRG_261:g.70803G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.2121G>A	ENSP00000502725.1:p.Glu707=
ENST00000392302.7:c.2121G>A	ENSP00000376120.3:p.Glu707=
ENST00000497019.7:c.*893G>A	ENSP00000436804.2:n.*893G>A
ENST00000524377.7:c.2301G>A MANE Select	ENSP00000431418.1:p.Glu767=
ENST00000531606.2:c.360G>A
ENST00000674537.1:c.2121G>A	ENSP00000502725.1:p.Glu707=
ENST00000358660.3:c.2292G>A	ENSP00000351486.3:p.Glu764=
ENST00000368196.7:c.2283G>A	ENSP00000357179.3:p.Glu761=
ENST00000392302.6:c.2193G>A	ENSP00000376120.2:p.Glu731=
ENST00000497019.6:c.*893G>A	ENSP00000436804.1:n.*893G>A
ENST00000524377.5:c.2301G>A	ENSP00000431418.1:p.Glu767=
ENST00000530298.5:n.2754G>A
ENST00000531606.1:n.344G>A
NM_001007792.1:c.2193G>A , LRG_261t1:c.2193G>A	NP_001007793.1:p.Glu731=
NM_001012331.1:c.2283G>A , LRG_261t2:c.2283G>A	NP_001012331.1:p.Glu761=
NM_002529.3:c.2301G>A , LRG_261t3:c.2301G>A	NP_002520.2:p.Glu767=
NM_001012331.2:c.2283G>A	NP_001012331.1:p.Glu761=
NM_002529.4:c.2301G>A MANE Select	NP_002520.2:p.Glu767=