Canonical Allele Identifier: CA2697276027

Gene: NTRK1

Linked Data

• dbSNP Id: rs1647900940

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156876292A>C , CM000663.2:g.156876292A>C	GRCh38
NC_000001.10:g.156846084A>C , CM000663.1:g.156846084A>C	GRCh37
NC_000001.9:g.155112708A>C	NCBI36
NG_007493.1:g.65543A>C , LRG_261:g.65543A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674537.2:c.1452+82A>C	ENSP00000502725.1:n.1452+82A>C
ENST00000392302.7:c.1452+82A>C	ENSP00000376120.3:n.1452+82A>C
ENST00000497019.7:c.*224+82A>C	ENSP00000436804.2:n.*224+82A>C
ENST00000524377.7:c.1632+82A>C MANE Select	ENSP00000431418.1:n.1632+82A>C
ENST00000674537.1:c.1452+82A>C	ENSP00000502725.1:n.1452+82A>C
ENST00000358660.3:c.1623+82A>C	ENSP00000351486.3:n.1623+82A>C
ENST00000368196.7:c.1614+82A>C	ENSP00000357179.3:n.1614+82A>C
ENST00000392302.6:c.1524+82A>C	ENSP00000376120.2:n.1524+82A>C
ENST00000497019.6:c.*224+82A>C	ENSP00000436804.1:n.*224+82A>C
ENST00000524377.5:c.1632+82A>C	ENSP00000431418.1:n.1632+82A>C
ENST00000530298.5:n.2085+82A>C
NM_001007792.1:c.1524+82A>C , LRG_261t1:c.1524+82A>C	NP_001007793.1:n.1524+82A>C
NM_001012331.1:c.1614+82A>C , LRG_261t2:c.1614+82A>C	NP_001012331.1:n.1614+82A>C
NM_002529.3:c.1632+82A>C , LRG_261t3:c.1632+82A>C	NP_002520.2:n.1632+82A>C
NM_001012331.2:c.1614+82A>C	NP_001012331.1:n.1614+82A>C
NM_002529.4:c.1632+82A>C MANE Select	NP_002520.2:n.1632+82A>C