Canonical Allele Identifier: CA1169464

Gene: NTRK1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876545G>A , CM000663.2:g.156876545G>A	GRCh38
NC_000001.10:g.156846337G>A , CM000663.1:g.156846337G>A	GRCh37
NC_000001.9:g.155112961G>A	NCBI36
NG_007493.1:g.65796G>A , LRG_261:g.65796G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1598G>A	ENSP00000502725.1:p.Arg533Gln
ENST00000392302.7:c.1598G>A	ENSP00000376120.3:p.Arg533Gln
ENST00000497019.7:c.*370G>A	ENSP00000436804.2:n.*370G>A
ENST00000524377.7:c.1778G>A MANE Select	ENSP00000431418.1:p.Arg593Gln
ENST00000674537.1:c.1598G>A	ENSP00000502725.1:p.Arg533Gln
ENST00000358660.3:c.1769G>A	ENSP00000351486.3:p.Arg590Gln
ENST00000368196.7:c.1760G>A	ENSP00000357179.3:p.Arg587Gln
ENST00000392302.6:c.1670G>A	ENSP00000376120.2:p.Arg557Gln
ENST00000497019.6:c.*370G>A	ENSP00000436804.1:n.*370G>A
ENST00000524377.5:c.1778G>A	ENSP00000431418.1:p.Arg593Gln
ENST00000530298.5:n.2231G>A
NM_001007792.1:c.1670G>A , LRG_261t1:c.1670G>A	NP_001007793.1:p.Arg557Gln
NM_001012331.1:c.1760G>A , LRG_261t2:c.1760G>A	NP_001012331.1:p.Arg587Gln
NM_002529.3:c.1778G>A , LRG_261t3:c.1778G>A	NP_002520.2:p.Arg593Gln
NM_001012331.2:c.1760G>A	NP_001012331.1:p.Arg587Gln
NM_002529.4:c.1778G>A MANE Select	NP_002520.2:p.Arg593Gln