Canonical Allele Identifier: CA10584140
Gene: NTRK1 HGNC NCBI

Linked Data

ClinVar Variation Id: 245653
ClinVar RCV Id: RCV000235671
dbSNP Id: rs879253890
MyVariant Identifiers: chr1:g.156845401A>T (hg19) chr1:g.156875609A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156875609A>T , CM000663.2:g.156875609A>T GRCh38
NC_000001.10:g.156845401A>T , CM000663.1:g.156845401A>T GRCh37
NC_000001.9:g.155112025A>T NCBI36
NG_007493.1:g.64860A>T , LRG_261:g.64860A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000674537.2:c.1264A>T ENSP00000502725.1:p.Lys422Ter
ENST00000392302.7:c.1264A>T ENSP00000376120.3:p.Lys422Ter
ENST00000497019.7:c.*36A>T ENSP00000436804.2:n.*36A>T
ENST00000524377.7:c.1444A>T MANE Select ENSP00000431418.1:p.Lys482Ter
ENST00000674537.1:c.1264A>T ENSP00000502725.1:p.Lys422Ter
ENST00000358660.3:c.1426A>T ENSP00000351486.3:p.Lys476Ter
ENST00000368196.7:c.1426A>T ENSP00000357179.3:p.Lys476Ter
ENST00000392302.6:c.1336A>T ENSP00000376120.2:p.Lys446Ter
ENST00000497019.6:c.*36A>T ENSP00000436804.1:n.*36A>T
ENST00000524377.5:c.1444A>T ENSP00000431418.1:p.Lys482Ter
ENST00000530298.5:n.1484A>T
ENST00000534682.1:n.667A>T
NM_001007792.1:c.1336A>T , LRG_261t1:c.1336A>T NP_001007793.1:p.Lys446Ter
NM_001012331.1:c.1426A>T , LRG_261t2:c.1426A>T NP_001012331.1:p.Lys476Ter
NM_002529.3:c.1444A>T , LRG_261t3:c.1444A>T NP_002520.2:p.Lys482Ter
NM_001012331.2:c.1426A>T NP_001012331.1:p.Lys476Ter
NM_002529.4:c.1444A>T MANE Select NP_002520.2:p.Lys482Ter
Search 100 bp 5'
Search 100 bp 3'