Canonical Allele Identifier: CA2697493458

Gene: NTRK1

Linked Data

• dbSNP Id: rs2102916825

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876034C>G , CM000663.2:g.156876034C>G	GRCh38
NC_000001.10:g.156845826C>G , CM000663.1:g.156845826C>G	GRCh37
NC_000001.9:g.155112450C>G	NCBI36
NG_007493.1:g.65285C>G , LRG_261:g.65285C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000674537.2:c.1322-46C>G	ENSP00000502725.1:n.1322-46C>G
ENST00000392302.7:c.1322-46C>G	ENSP00000376120.3:n.1322-46C>G
ENST00000497019.7:c.*94-46C>G	ENSP00000436804.2:n.*94-46C>G
ENST00000524377.7:c.1502-46C>G MANE Select	ENSP00000431418.1:n.1502-46C>G
ENST00000674537.1:c.1322-46C>G	ENSP00000502725.1:n.1322-46C>G
ENST00000358660.3:c.1484-37C>G	ENSP00000351486.3:n.1484-37C>G
ENST00000368196.7:c.1484-46C>G	ENSP00000357179.3:n.1484-46C>G
ENST00000392302.6:c.1394-46C>G	ENSP00000376120.2:n.1394-46C>G
ENST00000497019.6:c.*94-46C>G	ENSP00000436804.1:n.*94-46C>G
ENST00000524377.5:c.1502-46C>G	ENSP00000431418.1:n.1502-46C>G
ENST00000530298.5:n.1909C>G
ENST00000534682.1:n.725-46C>G
NM_001007792.1:c.1394-46C>G , LRG_261t1:c.1394-46C>G	NP_001007793.1:n.1394-46C>G
NM_001012331.1:c.1484-46C>G , LRG_261t2:c.1484-46C>G	NP_001012331.1:n.1484-46C>G
NM_002529.3:c.1502-46C>G , LRG_261t3:c.1502-46C>G	NP_002520.2:n.1502-46C>G
NM_001012331.2:c.1484-46C>G	NP_001012331.1:n.1484-46C>G
NM_002529.4:c.1502-46C>G MANE Select	NP_002520.2:n.1502-46C>G