Canonical Allele Identifier: CA1200786108
Gene: NTRK1 HGNC NCBI

Linked Data

dbSNP Id: rs1328029595

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156876475_156876480dup , CM000663.2:g.156876475_156876480dup GRCh38
NC_000001.10:g.156846267_156846272dup , CM000663.1:g.156846267_156846272dup GRCh37
NC_000001.9:g.155112891_155112896dup NCBI36
NG_007493.1:g.65726_65731dup , LRG_261:g.65726_65731dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.1528_1533dup ENSP00000502725.1:p.His511_Ile512insGlnHis
ENST00000392302.7:c.1528_1533dup ENSP00000376120.3:p.His511_Ile512insGlnHis
ENST00000497019.7:c.*300_*305dup ENSP00000436804.2:n.*300_*305dup
ENST00000524377.7:c.1708_1713dup MANE Select ENSP00000431418.1:p.His571_Ile572insGlnHis
ENST00000674537.1:c.1528_1533dup ENSP00000502725.1:p.His511_Ile512insGlnHis
ENST00000358660.3:c.1699_1704dup ENSP00000351486.3:p.His568_Ile569insGlnHis
ENST00000368196.7:c.1690_1695dup ENSP00000357179.3:p.His565_Ile566insGlnHis
ENST00000392302.6:c.1600_1605dup ENSP00000376120.2:p.His535_Ile536insGlnHis
ENST00000497019.6:c.*300_*305dup ENSP00000436804.1:n.*300_*305dup
ENST00000524377.5:c.1708_1713dup ENSP00000431418.1:p.His571_Ile572insGlnHis
ENST00000530298.5:n.2161_2166dup
NM_001007792.1:c.1600_1605dup , LRG_261t1:c.1600_1605dup NP_001007793.1:p.His535_Ile536insGlnHis
NM_001012331.1:c.1690_1695dup , LRG_261t2:c.1690_1695dup NP_001012331.1:p.His565_Ile566insGlnHis
NM_002529.3:c.1708_1713dup , LRG_261t3:c.1708_1713dup NP_002520.2:p.His571_Ile572insGlnHis
NM_001012331.2:c.1690_1695dup NP_001012331.1:p.His565_Ile566insGlnHis
NM_002529.4:c.1708_1713dup MANE Select NP_002520.2:p.His571_Ile572insGlnHis