Canonical Allele Identifier: CA1169069
Gene: NTRK1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.156868641G>A
GRCh37 chr1:g.156838433G>A
gnomAD v2:
1:156838433 G / A
gnomAD v3:
1:156868641 G / A
gnomAD v4:
chr1-156868641-G-A
Joint Max Group AF 0.00253606 (SAS)
Genomes Max Group AF 0.00207706 (SAS)
Exomes Max Group AF 0.00249995 (SAS)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156868641G>A , CM000663.2:g.156868641G>A GRCh38
NC_000001.10:g.156838433G>A , CM000663.1:g.156838433G>A GRCh37
NC_000001.9:g.155105057G>A NCBI36
NG_007493.1:g.57892G>A , LRG_261:g.57892G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.549G>A ENSP00000502725.1:p.Thr183=
ENST00000392302.7:c.549G>A ENSP00000376120.3:p.Thr183=
ENST00000497019.7:c.549G>A ENSP00000436804.2:p.Thr183=
ENST00000524377.7:c.711G>A MANE Select ENSP00000431418.1:p.Thr237=
ENST00000674537.1:c.549G>A ENSP00000502725.1:p.Thr183=
ENST00000358660.3:c.711G>A ENSP00000351486.3:p.Thr237=
ENST00000368196.7:c.711G>A ENSP00000357179.3:p.Thr237=
ENST00000392302.6:c.621G>A ENSP00000376120.2:p.Thr207=
ENST00000489021.6:n.313-4992G>A
ENST00000497019.6:c.621G>A ENSP00000436804.1:p.Thr207=
ENST00000524377.5:c.711G>A ENSP00000431418.1:p.Thr237=
ENST00000530298.5:n.769G>A
NM_001007792.1:c.621G>A , LRG_261t1:c.621G>A NP_001007793.1:p.Thr207=
NM_001012331.1:c.711G>A , LRG_261t2:c.711G>A NP_001012331.1:p.Thr237=
NM_002529.3:c.711G>A , LRG_261t3:c.711G>A NP_002520.2:p.Thr237=
NM_001012331.2:c.711G>A NP_001012331.1:p.Thr237=
NM_002529.4:c.711G>A MANE Select NP_002520.2:p.Thr237=
Search 100 bp 5'
Search 100 bp 3'