Canonical Allele Identifier: CA342937194

Gene: NTRK1

Linked Data

• dbSNP Id: rs1373141980
• COSMIC: COSM676352 ; COSM676353
• MyVariant Identifiers: chr1:g.156845314C>A (hg19) ; chr1:g.156875522C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156875522C>A , CM000663.2:g.156875522C>A	GRCh38
NC_000001.10:g.156845314C>A , CM000663.1:g.156845314C>A	GRCh37
NC_000001.9:g.155111938C>A	NCBI36
NG_007493.1:g.64773C>A , LRG_261:g.64773C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1177C>A	ENSP00000502725.1:p.Pro393Thr
ENST00000392302.7:c.1177C>A	ENSP00000376120.3:p.Pro393Thr
ENST00000497019.7:c.1044C>A	ENSP00000436804.2:p.Ala348=
ENST00000524377.7:c.1357C>A MANE Select	ENSP00000431418.1:p.Pro453Thr
ENST00000674537.1:c.1177C>A	ENSP00000502725.1:p.Pro393Thr
ENST00000358660.3:c.1339C>A	ENSP00000351486.3:p.Pro447Thr
ENST00000368196.7:c.1339C>A	ENSP00000357179.3:p.Pro447Thr
ENST00000392302.6:c.1249C>A	ENSP00000376120.2:p.Pro417Thr
ENST00000497019.6:c.1116C>A	ENSP00000436804.1:p.Ala372=
ENST00000524377.5:c.1357C>A	ENSP00000431418.1:p.Pro453Thr
ENST00000530298.5:n.1397C>A
ENST00000534682.1:n.580C>A
NM_001007792.1:c.1249C>A , LRG_261t1:c.1249C>A	NP_001007793.1:p.Pro417Thr
NM_001012331.1:c.1339C>A , LRG_261t2:c.1339C>A	NP_001012331.1:p.Pro447Thr
NM_002529.3:c.1357C>A , LRG_261t3:c.1357C>A	NP_002520.2:p.Pro453Thr
NM_001012331.2:c.1339C>A	NP_001012331.1:p.Pro447Thr
NM_002529.4:c.1357C>A MANE Select	NP_002520.2:p.Pro453Thr