Canonical Allele Identifier: CA1169571
Gene: NTRK1 HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156880071G>A , CM000663.2:g.156880071G>A GRCh38
NC_000001.10:g.156849863G>A , CM000663.1:g.156849863G>A GRCh37
NC_000001.9:g.155116487G>A NCBI36
NG_007493.1:g.69322G>A , LRG_261:g.69322G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.1939G>A ENSP00000502725.1:p.Glu647Lys
ENST00000392302.7:c.1939G>A ENSP00000376120.3:p.Glu647Lys
ENST00000497019.7:c.*711G>A ENSP00000436804.2:n.*711G>A
ENST00000524377.7:c.2119G>A MANE Select ENSP00000431418.1:p.Glu707Lys
ENST00000531606.2:c.87G>A
ENST00000674537.1:c.1939G>A ENSP00000502725.1:p.Glu647Lys
ENST00000358660.3:c.2110G>A ENSP00000351486.3:p.Glu704Lys
ENST00000368196.7:c.2101G>A ENSP00000357179.3:p.Glu701Lys
ENST00000392302.6:c.2011G>A ENSP00000376120.2:p.Glu671Lys
ENST00000497019.6:c.*711G>A ENSP00000436804.1:n.*711G>A
ENST00000524377.5:c.2119G>A ENSP00000431418.1:p.Glu707Lys
ENST00000530298.5:n.2572G>A
ENST00000531606.1:n.71G>A
NM_001007792.1:c.2011G>A , LRG_261t1:c.2011G>A NP_001007793.1:p.Glu671Lys
NM_001012331.1:c.2101G>A , LRG_261t2:c.2101G>A NP_001012331.1:p.Glu701Lys
NM_002529.3:c.2119G>A , LRG_261t3:c.2119G>A NP_002520.2:p.Glu707Lys
NM_001012331.2:c.2101G>A NP_001012331.1:p.Glu701Lys
NM_002529.4:c.2119G>A MANE Select NP_002520.2:p.Glu707Lys