Canonical Allele Identifier: CA645518199
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156876099_156876100delinsAT , CM000663.2:g.156876099_156876100delinsAT GRCh38
NC_000001.10:g.156845891_156845892delinsAT , CM000663.1:g.156845891_156845892delinsAT GRCh37
NC_000001.9:g.155112515_155112516delinsAT NCBI36
NG_007493.1:g.65350_65351delinsAT , LRG_261:g.65350_65351delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.1341_1342delinsAT ENSP00000502725.1:p.Arg448Trp
ENST00000392302.7:c.1341_1342delinsAT ENSP00000376120.3:p.Arg448Trp
ENST00000497019.7:c.*113_*114delinsAT ENSP00000436804.2:n.*113_*114delinsAT
ENST00000524377.7:c.1521_1522delinsAT MANE Select ENSP00000431418.1:p.Arg508Trp
ENST00000674537.1:c.1341_1342delinsAT ENSP00000502725.1:p.Arg448Trp
ENST00000358660.3:c.1512_1513delinsAT ENSP00000351486.3:p.Arg505Trp
ENST00000368196.7:c.1503_1504delinsAT ENSP00000357179.3:p.Arg502Trp
ENST00000392302.6:c.1413_1414delinsAT ENSP00000376120.2:p.Arg472Trp
ENST00000497019.6:c.*113_*114delinsAT ENSP00000436804.1:n.*113_*114delinsAT
ENST00000524377.5:c.1521_1522delinsAT ENSP00000431418.1:p.Arg508Trp
ENST00000530298.5:n.1974_1975delinsAT
ENST00000534682.1:n.744_745delinsAT
NM_001007792.1:c.1413_1414delinsAT , LRG_261t1:c.1413_1414delinsAT NP_001007793.1:p.Arg472Trp
NM_001012331.1:c.1503_1504delinsAT , LRG_261t2:c.1503_1504delinsAT NP_001012331.1:p.Arg502Trp
NM_002529.3:c.1521_1522delinsAT , LRG_261t3:c.1521_1522delinsAT NP_002520.2:p.Arg508Trp
NM_001012331.2:c.1503_1504delinsAT NP_001012331.1:p.Arg502Trp
NM_002529.4:c.1521_1522delinsAT MANE Select NP_002520.2:p.Arg508Trp