Canonical Allele Identifier: CA1140609711
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156866990C= , CM000663.2:g.156866990C= GRCh38
NC_000001.10:g.156836782C= , CM000663.1:g.156836782C= GRCh37
NC_000001.9:g.155103406C= NCBI36
NG_007493.1:g.56241C= , LRG_261:g.56241C=

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.266+12C= ENSP00000502725.1:n.266+12C=
ENST00000392302.7:c.266+12C= ENSP00000376120.3:n.266+12C=
ENST00000497019.7:c.266+12C= ENSP00000436804.2:n.266+12C=
ENST00000524377.7:c.428+12C= MANE Select ENSP00000431418.1:n.428+12C=
ENST00000674537.1:c.266+12C= ENSP00000502725.1:n.266+12C=
ENST00000358660.3:c.428+12C= ENSP00000351486.3:n.428+12C=
ENST00000368196.7:c.428+12C= ENSP00000357179.3:n.428+12C=
ENST00000392302.6:c.338+12C= ENSP00000376120.2:n.338+12C=
ENST00000489021.6:n.313-6643C=
ENST00000497019.6:c.338+12C= ENSP00000436804.1:n.338+12C=
ENST00000524377.5:c.428+12C= ENSP00000431418.1:n.428+12C=
ENST00000530298.5:n.486+12C=
NM_001007792.1:c.338+12C= , LRG_261t1:c.338+12C= NP_001007793.1:n.338+12C=
NM_001012331.1:c.428+12C= , LRG_261t2:c.428+12C= NP_001012331.1:n.428+12C=
NM_002529.3:c.428+12C= , LRG_261t3:c.428+12C= NP_002520.2:n.428+12C=
NM_001012331.2:c.428+12C= NP_001012331.1:n.428+12C=
NM_002529.4:c.428+12C= MANE Select NP_002520.2:n.428+12C=