Canonical Allele Identifier: CA1200784385
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156880023A= , CM000663.2:g.156880023A= GRCh38
NC_000001.10:g.156849815A= , CM000663.1:g.156849815A= GRCh37
NC_000001.9:g.155116439A= NCBI36
NG_007493.1:g.69274A= , LRG_261:g.69274A=

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1891A= ENSP00000502725.1:p.Ile631=
ENST00000392302.7:c.1891A= ENSP00000376120.3:p.Ile631=
ENST00000497019.7:c.*663A= ENSP00000436804.2:n.*663A=
ENST00000524377.7:c.2071A= MANE Select ENSP00000431418.1:p.Ile691=
ENST00000531606.2:c.39A=
ENST00000674537.1:c.1891A= ENSP00000502725.1:p.Ile631=
ENST00000358660.3:c.2062A= ENSP00000351486.3:p.Ile688=
ENST00000368196.7:c.2053A= ENSP00000357179.3:p.Ile685=
ENST00000392302.6:c.1963A= ENSP00000376120.2:p.Ile655=
ENST00000497019.6:c.*663A= ENSP00000436804.1:n.*663A=
ENST00000524377.5:c.2071A= ENSP00000431418.1:p.Ile691=
ENST00000530298.5:n.2524A=
ENST00000531606.1:n.23A=
NM_001007792.1:c.1963A= , LRG_261t1:c.1963A= NP_001007793.1:p.Ile655=
NM_001012331.1:c.2053A= , LRG_261t2:c.2053A= NP_001012331.1:p.Ile685=
NM_002529.3:c.2071A= , LRG_261t3:c.2071A= NP_002520.2:p.Ile691=
NM_001012331.2:c.2053A= NP_001012331.1:p.Ile685=
NM_002529.4:c.2071A= MANE Select NP_002520.2:p.Ile691=