Canonical Allele Identifier: CA342939529
Gene: NTRK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156879166T>A , CM000663.2:g.156879166T>A GRCh38
NC_000001.10:g.156848958T>A , CM000663.1:g.156848958T>A GRCh37
NC_000001.9:g.155115582T>A NCBI36
NG_007493.1:g.68417T>A , LRG_261:g.68417T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1670T>A ENSP00000502725.1:p.Val557Glu
ENST00000392302.7:c.1670T>A ENSP00000376120.3:p.Val557Glu
ENST00000497019.7:c.*442T>A ENSP00000436804.2:n.*442T>A
ENST00000524377.7:c.1850T>A MANE Select ENSP00000431418.1:p.Val617Glu
ENST00000674537.1:c.1670T>A ENSP00000502725.1:p.Val557Glu
ENST00000358660.3:c.1841T>A ENSP00000351486.3:p.Val614Glu
ENST00000368196.7:c.1832T>A ENSP00000357179.3:p.Val611Glu
ENST00000392302.6:c.1742T>A ENSP00000376120.2:p.Val581Glu
ENST00000497019.6:c.*442T>A ENSP00000436804.1:n.*442T>A
ENST00000524377.5:c.1850T>A ENSP00000431418.1:p.Val617Glu
ENST00000530298.5:n.2303T>A
NM_001007792.1:c.1742T>A , LRG_261t1:c.1742T>A NP_001007793.1:p.Val581Glu
NM_001012331.1:c.1832T>A , LRG_261t2:c.1832T>A NP_001012331.1:p.Val611Glu
NM_002529.3:c.1850T>A , LRG_261t3:c.1850T>A NP_002520.2:p.Val617Glu
NM_001012331.2:c.1832T>A NP_001012331.1:p.Val611Glu
NM_002529.4:c.1850T>A MANE Select NP_002520.2:p.Val617Glu