Canonical Allele Identifier: CA421138510

Gene: NTRK1

Linked Data

• ClinVar Variation Id: 1567704
• ClinVar RCV Id: RCV002210171
• dbSNP Id: rs774664479
• MyVariant Identifiers: chr1:g.156846209C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876417C>A , CM000663.2:g.156876417C>A	GRCh38
NC_000001.10:g.156846209C>A , CM000663.1:g.156846209C>A	GRCh37
NC_000001.9:g.155112833C>A	NCBI36
NG_007493.1:g.65668C>A , LRG_261:g.65668C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1470C>A	ENSP00000502725.1:p.Ser490=
ENST00000392302.7:c.1470C>A	ENSP00000376120.3:p.Ser490=
ENST00000497019.7:c.*242C>A	ENSP00000436804.2:n.*242C>A
ENST00000524377.7:c.1650C>A MANE Select	ENSP00000431418.1:p.Ser550=
ENST00000674537.1:c.1470C>A	ENSP00000502725.1:p.Ser490=
ENST00000358660.3:c.1641C>A	ENSP00000351486.3:p.Ser547=
ENST00000368196.7:c.1632C>A	ENSP00000357179.3:p.Ser544=
ENST00000392302.6:c.1542C>A	ENSP00000376120.2:p.Ser514=
ENST00000497019.6:c.*242C>A	ENSP00000436804.1:n.*242C>A
ENST00000524377.5:c.1650C>A	ENSP00000431418.1:p.Ser550=
ENST00000530298.5:n.2103C>A
NM_001007792.1:c.1542C>A , LRG_261t1:c.1542C>A	NP_001007793.1:p.Ser514=
NM_001012331.1:c.1632C>A , LRG_261t2:c.1632C>A	NP_001012331.1:p.Ser544=
NM_002529.3:c.1650C>A , LRG_261t3:c.1650C>A	NP_002520.2:p.Ser550=
NM_001012331.2:c.1632C>A	NP_001012331.1:p.Ser544=
NM_002529.4:c.1650C>A MANE Select	NP_002520.2:p.Ser550=