Canonical Allele Identifier: CA1200778622
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156860657C= , CM000663.2:g.156860657C= GRCh38
NC_000001.10:g.156830449C= , CM000663.1:g.156830449C= GRCh37
NC_000001.9:g.155097073C= NCBI36
NG_007493.1:g.49908C= , LRG_261:g.49908C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.51-3697C= ENSP00000502725.1:n.51-3697C=
ENST00000392302.7:c.51-3697C= ENSP00000376120.3:n.51-3697C=
ENST00000497019.7:c.51-3697C= ENSP00000436804.2:n.51-3697C=
ENST00000674537.1:c.51-3697C= ENSP00000502725.1:n.51-3697C=
ENST00000392302.6:c.123-3697C= ENSP00000376120.2:n.123-3697C=
ENST00000489021.6:n.313-12976C=
ENST00000497019.6:c.123-3697C= ENSP00000436804.1:n.123-3697C=
ENST00000530298.5:n.271-3697C=
NM_001007792.1:c.123-3697C= , LRG_261t1:c.123-3697C= NP_001007793.1:n.123-3697C=