Canonical Allele Identifier: CA204920

Gene: NTRK1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156873600T>A , CM000663.2:g.156873600T>A	GRCh38
NC_000001.10:g.156843392T>A , CM000663.1:g.156843392T>A	GRCh37
NC_000001.9:g.155110016T>A	NCBI36
NG_007493.1:g.62851T>A , LRG_261:g.62851T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.689-33T>A	ENSP00000502725.1:n.689-33T>A
ENST00000392302.7:c.689-33T>A	ENSP00000376120.3:n.689-33T>A
ENST00000497019.7:c.556-33T>A	ENSP00000436804.2:n.556-33T>A
ENST00000524377.7:c.851-33T>A MANE Select	ENSP00000431418.1:n.851-33T>A
ENST00000674537.1:c.689-33T>A	ENSP00000502725.1:n.689-33T>A
ENST00000358660.3:c.851-33T>A	ENSP00000351486.3:n.851-33T>A
ENST00000368196.7:c.851-33T>A	ENSP00000357179.3:n.851-33T>A
ENST00000392302.6:c.761-33T>A	ENSP00000376120.2:n.761-33T>A
ENST00000489021.6:n.313-33T>A
ENST00000497019.6:c.628-33T>A	ENSP00000436804.1:n.628-33T>A
ENST00000524377.5:c.851-33T>A	ENSP00000431418.1:n.851-33T>A
ENST00000530298.5:n.909-33T>A
NM_001007792.1:c.761-33T>A , LRG_261t1:c.761-33T>A	NP_001007793.1:n.761-33T>A
NM_001012331.1:c.851-33T>A , LRG_261t2:c.851-33T>A	NP_001012331.1:n.851-33T>A
NM_002529.3:c.851-33T>A , LRG_261t3:c.851-33T>A	NP_002520.2:n.851-33T>A
NM_001012331.2:c.851-33T>A	NP_001012331.1:n.851-33T>A
NM_002529.4:c.851-33T>A MANE Select	NP_002520.2:n.851-33T>A