Canonical Allele Identifier: CA7717414
Gene: NTRK3 HGNC NCBI
NTRK3-AS1 HGNC NCBI
MyVariant.info:
Revel Score:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.88256017C>G , CM000677.2:g.88256017C>G GRCh38
NC_000015.9:g.88799248C>G , CM000677.1:g.88799248C>G GRCh37
NC_000015.8:g.86600252C>G NCBI36
NG_029619.1:g.5715G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000317501.9:c.137G>C (NTRK3) ENSP00000318328.3:p.Arg46Pro
ENST00000629765.3:c.137G>C (NTRK3) MANE Select ENSP00000485864.1:p.Arg46Pro
ENST00000695462.1:c.137G>C (NTRK3) ENSP00000511942.1:p.Arg46Pro
ENST00000695463.1:c.-158G>C (NTRK3) ENSP00000511943.1:n.-158G>C
ENST00000317501.7:c.137G>C (NTRK3) ENSP00000318328.3:p.Arg46Pro
ENST00000355254.6:c.137G>C (NTRK3) ENSP00000347397.3:p.Arg46Pro
ENST00000357724.6:c.137G>C (NTRK3) ENSP00000350356.2:p.Arg46Pro
ENST00000360948.6:c.137G>C (NTRK3) ENSP00000354207.2:p.Arg46Pro
ENST00000394480.6:c.137G>C (NTRK3) ENSP00000377990.1:p.Arg46Pro
ENST00000540489.6:c.137G>C (NTRK3) ENSP00000444673.2:p.Arg46Pro
ENST00000557856.5:c.137G>C (NTRK3) ENSP00000453959.1:p.Arg46Pro
ENST00000558676.5:c.137G>C (NTRK3) ENSP00000453511.1:p.Arg46Pro
ENST00000559067.1:n.443G>C (NTRK3)
ENST00000626019.2:c.137G>C (NTRK3) ENSP00000486784.1:p.Arg46Pro
ENST00000629765.2:c.137G>C (NTRK3) ENSP00000485864.1:p.Arg46Pro
NM_001007156.2:c.137G>C (NTRK3) NP_001007157.1:p.Arg46Pro
NM_001012338.2:c.137G>C (NTRK3) NP_001012338.1:p.Arg46Pro
NM_001243101.1:c.137G>C (NTRK3) NP_001230030.1:p.Arg46Pro
NM_002530.3:c.137G>C (NTRK3) NP_002521.2:p.Arg46Pro
NR_038229.1:n.749+2539C>G (NTRK3-AS1)
XM_006720543.2:c.137G>C (NTRK3) XP_006720606.1:p.Arg46Pro
XM_006720544.2:c.137G>C (NTRK3) XP_006720607.1:p.Arg46Pro
XM_006720545.2:c.137G>C (NTRK3) XP_006720608.1:p.Arg46Pro
XM_006720546.2:c.137G>C (NTRK3) XP_006720609.1:p.Arg46Pro
XM_006720547.2:c.137G>C (NTRK3) XP_006720610.1:p.Arg46Pro
XM_006720548.2:c.137G>C (NTRK3) XP_006720611.1:p.Arg46Pro
XM_006720549.2:c.137G>C (NTRK3) XP_006720612.1:p.Arg46Pro
XM_006720550.2:c.137G>C (NTRK3) XP_006720613.1:p.Arg46Pro
XM_011521634.1:c.137G>C (NTRK3) XP_011519936.1:p.Arg46Pro
XM_011521635.1:c.137G>C (NTRK3) XP_011519937.1:p.Arg46Pro
XM_011521637.1:c.137G>C (NTRK3) XP_011519939.1:p.Arg46Pro
XM_011521638.1:c.137G>C (NTRK3) XP_011519940.1:p.Arg46Pro
XR_931841.1:n.200G>C (NTRK3)
XR_931842.1:n.200G>C (NTRK3)
NM_001320134.1:c.137G>C (NTRK3) NP_001307063.1:p.Arg46Pro
XM_006720543.4:c.137G>C (NTRK3) XP_006720606.1:p.Arg46Pro
XM_006720544.4:c.137G>C (NTRK3) XP_006720607.1:p.Arg46Pro
XM_006720545.4:c.137G>C (NTRK3) XP_006720608.1:p.Arg46Pro
XM_006720548.4:c.137G>C (NTRK3) XP_006720611.1:p.Arg46Pro
XM_006720549.4:c.137G>C (NTRK3) XP_006720612.1:p.Arg46Pro
XM_006720550.4:c.137G>C (NTRK3) XP_006720613.1:p.Arg46Pro
XM_011521637.3:c.137G>C (NTRK3) XP_011519939.1:p.Arg46Pro
XM_011521638.3:c.137G>C (NTRK3) XP_011519940.1:p.Arg46Pro
XM_017022240.1:c.137G>C (NTRK3) XP_016877729.1:p.Arg46Pro
XM_017022242.2:c.137G>C (NTRK3) XP_016877731.1:p.Arg46Pro
XM_017022247.2:c.137G>C (NTRK3) XP_016877736.1:p.Arg46Pro
XM_017022248.2:c.137G>C (NTRK3) XP_016877737.1:p.Arg46Pro
XM_017022250.2:c.137G>C (NTRK3) XP_016877739.1:p.Arg46Pro
XM_017022253.2:c.137G>C (NTRK3) XP_016877742.1:p.Arg46Pro
XM_017022254.2:c.137G>C (NTRK3) XP_016877743.1:p.Arg46Pro
XM_024449934.1:c.137G>C (NTRK3) XP_024305702.1:p.Arg46Pro
XM_024449935.1:c.137G>C (NTRK3) XP_024305703.1:p.Arg46Pro
XR_001751292.2:n.780G>C (NTRK3)
XR_001751293.2:n.775G>C (NTRK3)
XR_002957645.1:n.776G>C (NTRK3)
NM_001375810.1:c.137G>C (NTRK3) NP_001362739.1:p.Arg46Pro
NM_001375811.1:c.137G>C (NTRK3) NP_001362740.1:p.Arg46Pro
NM_001375812.1:c.137G>C (NTRK3) NP_001362741.1:p.Arg46Pro
NM_001375813.1:c.137G>C (NTRK3) NP_001362742.1:p.Arg46Pro
NM_001375814.1:c.137G>C (NTRK3) NP_001362743.1:p.Arg46Pro
NM_002530.4:c.137G>C (NTRK3) NP_002521.2:p.Arg46Pro
NM_001007156.3:c.137G>C (NTRK3) NP_001007157.1:p.Arg46Pro
NM_001012338.3:c.137G>C (NTRK3) MANE Select NP_001012338.1:p.Arg46Pro
NM_001243101.2:c.137G>C (NTRK3) NP_001230030.1:p.Arg46Pro