Canonical Allele Identifier: CA342938678

Gene: NTRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876540T>G , CM000663.2:g.156876540T>G	GRCh38
NC_000001.10:g.156846332T>G , CM000663.1:g.156846332T>G	GRCh37
NC_000001.9:g.155112956T>G	NCBI36
NG_007493.1:g.65791T>G , LRG_261:g.65791T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002529.4:c.1773T>G MANE Select	NP_002520.2:p.Tyr591Ter
ENST00000524377.7:c.1773T>G MANE Select	ENSP00000431418.1:p.Tyr591Ter
NM_001007792.1:c.1665T>G , LRG_261t1:c.1665T>G	NP_001007793.1:p.Tyr555Ter
NM_001012331.1:c.1755T>G , LRG_261t2:c.1755T>G	NP_001012331.1:p.Tyr585Ter
NM_001012331.2:c.1755T>G	NP_001012331.1:p.Tyr585Ter
NM_002529.3:c.1773T>G , LRG_261t3:c.1773T>G	NP_002520.2:p.Tyr591Ter
ENST00000358660.3:c.1764T>G	ENSP00000351486.3:p.Tyr588Ter
ENST00000368196.7:c.1755T>G	ENSP00000357179.3:p.Tyr585Ter
ENST00000392302.6:c.1665T>G	ENSP00000376120.2:p.Tyr555Ter
ENST00000392302.7:c.1593T>G	ENSP00000376120.3:p.Tyr531Ter
ENST00000497019.6:c.*365T>G	ENSP00000436804.1:n.*365T>G
ENST00000497019.7:c.*365T>G	ENSP00000436804.2:n.*365T>G
ENST00000524377.5:c.1773T>G	ENSP00000431418.1:p.Tyr591Ter
ENST00000530298.5:n.2226T>G
ENST00000674537.1:c.1593T>G	ENSP00000502725.1:p.Tyr531Ter
ENST00000674537.2:c.1593T>G	ENSP00000502725.1:p.Tyr531Ter