Canonical Allele Identifier: CA1200778755
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156860875C= , CM000663.2:g.156860875C= GRCh38
NC_000001.10:g.156830667C= , CM000663.1:g.156830667C= GRCh37
NC_000001.9:g.155097291C= NCBI36
NG_007493.1:g.50126C= , LRG_261:g.50126C=

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.51-3479C= ENSP00000502725.1:n.51-3479C=
ENST00000392302.7:c.51-3479C= ENSP00000376120.3:n.51-3479C=
ENST00000497019.7:c.51-3479C= ENSP00000436804.2:n.51-3479C=
ENST00000524377.7:c.-60C= MANE Select ENSP00000431418.1:n.-60C=
ENST00000674537.1:c.51-3479C= ENSP00000502725.1:n.51-3479C=
ENST00000368196.7:c.-60C= ENSP00000357179.3:n.-60C=
ENST00000392302.6:c.123-3479C= ENSP00000376120.2:n.123-3479C=
ENST00000489021.6:n.313-12758C=
ENST00000497019.6:c.123-3479C= ENSP00000436804.1:n.123-3479C=
ENST00000530298.5:n.271-3479C=
NM_001007792.1:c.123-3479C= , LRG_261t1:c.123-3479C= NP_001007793.1:n.123-3479C=
NM_001012331.2:c.-60C= NP_001012331.1:n.-60C=
NM_002529.4:c.-60C= MANE Select NP_002520.2:n.-60C=