Canonical Allele Identifier: CA2841934573
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156881399dup , CM000663.2:g.156881399dup GRCh38
NC_000001.10:g.156851191dup , CM000663.1:g.156851191dup GRCh37
NC_000001.9:g.155117815dup NCBI36
NG_007493.1:g.70650dup , LRG_261:g.70650dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.2026-58dup ENSP00000502725.1:n.2026-58dup
ENST00000392302.7:c.2026-58dup ENSP00000376120.3:n.2026-58dup
ENST00000497019.7:c.*798-58dup ENSP00000436804.2:n.*798-58dup
ENST00000524377.7:c.2206-58dup MANE Select ENSP00000431418.1:n.2206-58dup
ENST00000531606.2:c.265-58dup
ENST00000674537.1:c.2026-58dup ENSP00000502725.1:n.2026-58dup
ENST00000358660.3:c.2197-58dup ENSP00000351486.3:n.2197-58dup
ENST00000368196.7:c.2188-58dup ENSP00000357179.3:n.2188-58dup
ENST00000392302.6:c.2098-58dup ENSP00000376120.2:n.2098-58dup
ENST00000497019.6:c.*798-58dup ENSP00000436804.1:n.*798-58dup
ENST00000524377.5:c.2206-58dup ENSP00000431418.1:n.2206-58dup
ENST00000530298.5:n.2659-58dup
ENST00000531606.1:n.249-58dup
NM_001007792.1:c.2098-58dup , LRG_261t1:c.2098-58dup NP_001007793.1:n.2098-58dup
NM_001012331.1:c.2188-58dup , LRG_261t2:c.2188-58dup NP_001012331.1:n.2188-58dup
NM_002529.3:c.2206-58dup , LRG_261t3:c.2206-58dup NP_002520.2:n.2206-58dup
NM_001012331.2:c.2188-58dup NP_001012331.1:n.2188-58dup
NM_002529.4:c.2206-58dup MANE Select NP_002520.2:n.2206-58dup