Canonical Allele Identifier: CA2648463145
Gene: NTRK1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156875934G>T , CM000663.2:g.156875934G>T GRCh38
NC_000001.10:g.156845726G>T , CM000663.1:g.156845726G>T GRCh37
NC_000001.9:g.155112350G>T NCBI36
NG_007493.1:g.65185G>T , LRG_261:g.65185G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.1322-146G>T ENSP00000502725.1:n.1322-146G>T
ENST00000392302.7:c.1322-146G>T ENSP00000376120.3:n.1322-146G>T
ENST00000497019.7:c.*94-146G>T ENSP00000436804.2:n.*94-146G>T
ENST00000524377.7:c.1502-146G>T MANE Select ENSP00000431418.1:n.1502-146G>T
ENST00000674537.1:c.1322-146G>T ENSP00000502725.1:n.1322-146G>T
ENST00000358660.3:c.1484-137G>T ENSP00000351486.3:n.1484-137G>T
ENST00000368196.7:c.1484-146G>T ENSP00000357179.3:n.1484-146G>T
ENST00000392302.6:c.1394-146G>T ENSP00000376120.2:n.1394-146G>T
ENST00000497019.6:c.*94-146G>T ENSP00000436804.1:n.*94-146G>T
ENST00000524377.5:c.1502-146G>T ENSP00000431418.1:n.1502-146G>T
ENST00000530298.5:n.1809G>T
ENST00000534682.1:n.725-146G>T
NM_001007792.1:c.1394-146G>T , LRG_261t1:c.1394-146G>T NP_001007793.1:n.1394-146G>T
NM_001012331.1:c.1484-146G>T , LRG_261t2:c.1484-146G>T NP_001012331.1:n.1484-146G>T
NM_002529.3:c.1502-146G>T , LRG_261t3:c.1502-146G>T NP_002520.2:n.1502-146G>T
NM_001012331.2:c.1484-146G>T NP_001012331.1:n.1484-146G>T
NM_002529.4:c.1502-146G>T MANE Select NP_002520.2:n.1502-146G>T
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