Canonical Allele Identifier: CA2648465702
Gene: NTRK1 HGNC NCBI

Linked Data

dbSNP Id: rs2102926624

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156879925G>T , CM000663.2:g.156879925G>T GRCh38
NC_000001.10:g.156849717G>T , CM000663.1:g.156849717G>T GRCh37
NC_000001.9:g.155116341G>T NCBI36
NG_007493.1:g.69176G>T , LRG_261:g.69176G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1867-74G>T ENSP00000502725.1:n.1867-74G>T
ENST00000392302.7:c.1867-74G>T ENSP00000376120.3:n.1867-74G>T
ENST00000497019.7:c.*639-74G>T ENSP00000436804.2:n.*639-74G>T
ENST00000524377.7:c.2047-74G>T MANE Select ENSP00000431418.1:n.2047-74G>T
ENST00000531606.2:c.15-74G>T
ENST00000674537.1:c.1867-74G>T ENSP00000502725.1:n.1867-74G>T
ENST00000358660.3:c.2038-74G>T ENSP00000351486.3:n.2038-74G>T
ENST00000368196.7:c.2029-74G>T ENSP00000357179.3:n.2029-74G>T
ENST00000392302.6:c.1939-74G>T ENSP00000376120.2:n.1939-74G>T
ENST00000497019.6:c.*639-74G>T ENSP00000436804.1:n.*639-74G>T
ENST00000524377.5:c.2047-74G>T ENSP00000431418.1:n.2047-74G>T
ENST00000530298.5:n.2500-74G>T
NM_001007792.1:c.1939-74G>T , LRG_261t1:c.1939-74G>T NP_001007793.1:n.1939-74G>T
NM_001012331.1:c.2029-74G>T , LRG_261t2:c.2029-74G>T NP_001012331.1:n.2029-74G>T
NM_002529.3:c.2047-74G>T , LRG_261t3:c.2047-74G>T NP_002520.2:n.2047-74G>T
NM_001012331.2:c.2029-74G>T NP_001012331.1:n.2029-74G>T
NM_002529.4:c.2047-74G>T MANE Select NP_002520.2:n.2047-74G>T