Canonical Allele Identifier: CA2630181259

Gene: NTRK3

Linked Data

• gnomAD v4: 15-87977740-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87977744del , CM000677.2:g.87977744del	GRCh38
NC_000015.9:g.88520975del , CM000677.1:g.88520975del	GRCh37
NC_000015.8:g.86321979del	NCBI36
NG_029619.1:g.283991del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317501.9:c.*1604del	ENSP00000318328.3:n.*1604del
ENST00000629765.3:c.1586-36988del MANE Select	ENSP00000485864.1:n.1586-36988del
ENST00000695462.1:c.1586-36988del	ENSP00000511942.1:n.1586-36988del
ENST00000695463.1:c.*1604del	ENSP00000511943.1:n.*1604del
ENST00000317501.7:c.*1604del	ENSP00000318328.3:n.*1604del
ENST00000355254.6:c.1562-36988del	ENSP00000347397.3:n.1562-36988del
ENST00000357724.6:c.1562-36988del	ENSP00000350356.2:n.1562-36988del
ENST00000360948.6:c.1586-36988del	ENSP00000354207.2:n.1586-36988del
ENST00000394480.6:c.1586-36988del	ENSP00000377990.1:n.1586-36988del
ENST00000542733.6:c.1292-36988del	ENSP00000437773.2:n.1292-36988del
ENST00000557856.5:c.1562-36988del	ENSP00000453959.1:n.1562-36988del
ENST00000558676.5:c.1562-36988del	ENSP00000453511.1:n.1562-36988del
ENST00000560201.1:n.200-150del
ENST00000626019.2:c.1586-36988del	ENSP00000486784.1:n.1586-36988del
ENST00000629765.2:c.1586-36988del	ENSP00000485864.1:n.1586-36988del
NM_001007156.2:c.*1604del	NP_001007157.1:n.*1604del
NM_001012338.2:c.1586-36988del	NP_001012338.1:n.1586-36988del
NM_001243101.1:c.1562-36988del	NP_001230030.1:n.1562-36988del
NM_002530.3:c.1586-36988del	NP_002521.2:n.1586-36988del
XM_006720543.2:c.1586-36988del	XP_006720606.1:n.1586-36988del
XM_006720544.2:c.1562-36988del	XP_006720607.1:n.1562-36988del
XM_006720545.2:c.1586-36988del	XP_006720608.1:n.1586-36988del
XM_006720546.2:c.*1604del	XP_006720609.1:n.*1604del
XM_011521634.1:c.1586-36988del	XP_011519936.1:n.1586-36988del
XM_011521635.1:c.1586-36988del	XP_011519937.1:n.1586-36988del
XM_011521636.1:c.1292-36988del	XP_011519938.1:n.1292-36988del
XM_011521637.1:c.*1604del	XP_011519939.1:n.*1604del
XR_931841.1:n.1788-36988del
NM_001320134.1:c.*1604del	NP_001307063.1:n.*1604del
NM_001320135.1:c.1292-36988del	NP_001307064.1:n.1292-36988del
XM_006720543.4:c.1586-36988del	XP_006720606.1:n.1586-36988del
XM_006720544.4:c.1562-36988del	XP_006720607.1:n.1562-36988del
XM_006720545.4:c.1586-36988del	XP_006720608.1:n.1586-36988del
XM_011521637.3:c.*1604del	XP_011519939.1:n.*1604del
XM_017022240.1:c.1586-36988del	XP_016877729.1:n.1586-36988del
XM_017022241.1:c.1400-36988del	XP_016877730.1:n.1400-36988del
XM_017022242.2:c.1586-36988del	XP_016877731.1:n.1586-36988del
XM_017022243.1:c.1292-36988del	XP_016877732.1:n.1292-36988del
XM_017022244.2:c.1292-36988del	XP_016877733.1:n.1292-36988del
XM_017022245.2:c.1292-36988del	XP_016877734.1:n.1292-36988del
XM_017022247.2:c.*1604del	XP_016877736.1:n.*1604del
XM_017022248.2:c.*1604del	XP_016877737.1:n.*1604del
XM_017022251.2:c.479-36988del	XP_016877740.1:n.479-36988del
XM_017022252.2:c.455-36988del	XP_016877741.1:n.455-36988del
XM_017022253.2:c.1586-36988del	XP_016877742.1:n.1586-36988del
XM_017022254.2:c.1586-36988del	XP_016877743.1:n.1586-36988del
XM_024449933.1:c.1268-36988del	XP_024305701.1:n.1268-36988del
XM_024449934.1:c.*1604del	XP_024305702.1:n.*1604del
XM_024449936.1:c.*1604del	XP_024305704.1:n.*1604del
XR_001751292.2:n.2229-36988del
NM_001375810.1:c.1586-36988del	NP_001362739.1:n.1586-36988del
NM_001375811.1:c.1586-36988del	NP_001362740.1:n.1586-36988del
NM_001375812.1:c.1562-36988del	NP_001362741.1:n.1562-36988del
NM_001375813.1:c.*1604del	NP_001362742.1:n.*1604del
NM_001375814.1:c.*1604del	NP_001362743.1:n.*1604del
NM_002530.4:c.1586-36988del	NP_002521.2:n.1586-36988del
NM_001007156.3:c.*1604del	NP_001007157.1:n.*1604del
NM_001012338.3:c.1586-36988del MANE Select	NP_001012338.1:n.1586-36988del
NM_001243101.2:c.1562-36988del	NP_001230030.1:n.1562-36988del
NM_001320135.2:c.1292-36988del	NP_001307064.1:n.1292-36988del