Canonical Allele Identifier: CA393914380
Community Standard Title: NM_001012338.3(NTRK3):c.1867G>A (p.Gly623Arg)
Gene: NTRK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87933034C>T , CM000677.2:g.87933034C>T GRCh38
NC_000015.9:g.88476265C>T , CM000677.1:g.88476265C>T GRCh37
NC_000015.8:g.86277269C>T NCBI36
NG_029619.1:g.328698G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001012338.3:c.1867G>A MANE Select NP_001012338.1:p.Gly623Arg
ENST00000629765.3:c.1867G>A MANE Select ENSP00000485864.1:p.Gly623Arg
NM_001012338.2:c.1867G>A NP_001012338.1:p.Gly623Arg
NM_001243101.1:c.1843G>A NP_001230030.1:p.Gly615Arg
NM_001243101.2:c.1843G>A NP_001230030.1:p.Gly615Arg
NM_001320135.1:c.1573G>A NP_001307064.1:p.Gly525Arg
NM_001320135.2:c.1573G>A NP_001307064.1:p.Gly525Arg
NM_001375810.1:c.1867G>A NP_001362739.1:p.Gly623Arg
NM_001375811.1:c.1867G>A NP_001362740.1:p.Gly623Arg
NM_001375812.1:c.1843G>A NP_001362741.1:p.Gly615Arg
NM_002530.3:c.1867G>A NP_002521.2:p.Gly623Arg
NM_002530.4:c.1867G>A NP_002521.2:p.Gly623Arg
ENST00000355254.6:c.1843G>A ENSP00000347397.3:p.Gly615Arg
ENST00000357724.6:c.1843G>A ENSP00000350356.2:p.Gly615Arg
ENST00000360948.6:c.1867G>A ENSP00000354207.2:p.Gly623Arg
ENST00000394480.6:c.1867G>A ENSP00000377990.1:p.Gly623Arg
ENST00000542733.6:c.1573G>A ENSP00000437773.2:p.Gly525Arg
ENST00000557856.5:c.1843G>A ENSP00000453959.1:p.Gly615Arg
ENST00000558576.5:c.57G>A
ENST00000558676.5:c.1843G>A ENSP00000453511.1:p.Gly615Arg
ENST00000559680.1:n.264G>A
ENST00000626019.2:c.1867G>A ENSP00000486784.1:p.Gly623Arg
ENST00000629765.2:c.1867G>A ENSP00000485864.1:p.Gly623Arg
ENST00000695462.1:c.1867G>A ENSP00000511942.1:p.Gly623Arg
XM_006720543.2:c.1867G>A XP_006720606.1:p.Gly623Arg
XM_006720543.4:c.1867G>A XP_006720606.1:p.Gly623Arg
XM_006720544.2:c.1843G>A XP_006720607.1:p.Gly615Arg
XM_006720544.4:c.1843G>A XP_006720607.1:p.Gly615Arg
XM_006720545.2:c.1867G>A XP_006720608.1:p.Gly623Arg
XM_006720545.4:c.1867G>A XP_006720608.1:p.Gly623Arg
XM_011521634.1:c.1867G>A XP_011519936.1:p.Gly623Arg
XM_011521635.1:c.1867G>A XP_011519937.1:p.Gly623Arg
XM_011521636.1:c.1573G>A XP_011519938.1:p.Gly525Arg
XM_017022240.1:c.1867G>A XP_016877729.1:p.Gly623Arg
XM_017022241.1:c.1681G>A XP_016877730.1:p.Gly561Arg
XM_017022242.2:c.1867G>A XP_016877731.1:p.Gly623Arg
XM_017022243.1:c.1573G>A XP_016877732.1:p.Gly525Arg
XM_017022244.2:c.1573G>A XP_016877733.1:p.Gly525Arg
XM_017022245.2:c.1573G>A XP_016877734.1:p.Gly525Arg
XM_017022251.2:c.760G>A XP_016877740.1:p.Gly254Arg
XM_017022252.2:c.736G>A XP_016877741.1:p.Gly246Arg
XM_017022253.2:c.1867G>A XP_016877742.1:p.Gly623Arg
XM_017022254.2:c.1867G>A XP_016877743.1:p.Gly623Arg
XM_024449933.1:c.1549G>A XP_024305701.1:p.Gly517Arg
XR_001751292.2:n.2510G>A
XR_931841.1:n.2069G>A