Canonical Allele Identifier: CA421138921

Gene: NTRK1

Linked Data

• dbSNP Id: rs1057290550
• MyVariant Identifiers: chr1:g.156846305C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876513C>G , CM000663.2:g.156876513C>G	GRCh38
NC_000001.10:g.156846305C>G , CM000663.1:g.156846305C>G	GRCh37
NC_000001.9:g.155112929C>G	NCBI36
NG_007493.1:g.65764C>G , LRG_261:g.65764C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1566C>G	ENSP00000502725.1:p.Gly522=
ENST00000392302.7:c.1566C>G	ENSP00000376120.3:p.Gly522=
ENST00000497019.7:c.*338C>G	ENSP00000436804.2:n.*338C>G
ENST00000524377.7:c.1746C>G MANE Select	ENSP00000431418.1:p.Gly582=
ENST00000674537.1:c.1566C>G	ENSP00000502725.1:p.Gly522=
ENST00000358660.3:c.1737C>G	ENSP00000351486.3:p.Gly579=
ENST00000368196.7:c.1728C>G	ENSP00000357179.3:p.Gly576=
ENST00000392302.6:c.1638C>G	ENSP00000376120.2:p.Gly546=
ENST00000497019.6:c.*338C>G	ENSP00000436804.1:n.*338C>G
ENST00000524377.5:c.1746C>G	ENSP00000431418.1:p.Gly582=
ENST00000530298.5:n.2199C>G
NM_001007792.1:c.1638C>G , LRG_261t1:c.1638C>G	NP_001007793.1:p.Gly546=
NM_001012331.1:c.1728C>G , LRG_261t2:c.1728C>G	NP_001012331.1:p.Gly576=
NM_002529.3:c.1746C>G , LRG_261t3:c.1746C>G	NP_002520.2:p.Gly582=
NM_001012331.2:c.1728C>G	NP_001012331.1:p.Gly576=
NM_002529.4:c.1746C>G MANE Select	NP_002520.2:p.Gly582=