Canonical Allele Identifier: CA2648463302

Gene: NTRK1

Linked Data

• gnomAD v4: 1-156876045-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876045C>A , CM000663.2:g.156876045C>A	GRCh38
NC_000001.10:g.156845837C>A , CM000663.1:g.156845837C>A	GRCh37
NC_000001.9:g.155112461C>A	NCBI36
NG_007493.1:g.65296C>A , LRG_261:g.65296C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1322-35C>A	ENSP00000502725.1:n.1322-35C>A
ENST00000392302.7:c.1322-35C>A	ENSP00000376120.3:n.1322-35C>A
ENST00000497019.7:c.*94-35C>A	ENSP00000436804.2:n.*94-35C>A
ENST00000524377.7:c.1502-35C>A MANE Select	ENSP00000431418.1:n.1502-35C>A
ENST00000674537.1:c.1322-35C>A	ENSP00000502725.1:n.1322-35C>A
ENST00000358660.3:c.1484-26C>A	ENSP00000351486.3:n.1484-26C>A
ENST00000368196.7:c.1484-35C>A	ENSP00000357179.3:n.1484-35C>A
ENST00000392302.6:c.1394-35C>A	ENSP00000376120.2:n.1394-35C>A
ENST00000497019.6:c.*94-35C>A	ENSP00000436804.1:n.*94-35C>A
ENST00000524377.5:c.1502-35C>A	ENSP00000431418.1:n.1502-35C>A
ENST00000530298.5:n.1920C>A
ENST00000534682.1:n.725-35C>A
NM_001007792.1:c.1394-35C>A , LRG_261t1:c.1394-35C>A	NP_001007793.1:n.1394-35C>A
NM_001012331.1:c.1484-35C>A , LRG_261t2:c.1484-35C>A	NP_001012331.1:n.1484-35C>A
NM_002529.3:c.1502-35C>A , LRG_261t3:c.1502-35C>A	NP_002520.2:n.1502-35C>A
NM_001012331.2:c.1484-35C>A	NP_001012331.1:n.1484-35C>A
NM_002529.4:c.1502-35C>A MANE Select	NP_002520.2:n.1502-35C>A