Canonical Allele Identifier: CA274416724

Gene: NTRK3

Linked Data

• dbSNP Id: rs138279532
• gnomAD v3: 15-88121463-T-C
• gnomAD v4: 15-88121463-T-C
• MyVariant Identifiers: chr15:g.88664694T>C (hg19) ; chr15:g.88121463T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.88121463T>C , CM000677.2:g.88121463T>C	GRCh38
NC_000015.9:g.88664694T>C , CM000677.1:g.88664694T>C	GRCh37
NC_000015.8:g.86465698T>C	NCBI36
NG_029619.1:g.140269A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317501.9:c.1396+4808A>G	ENSP00000318328.3:n.1396+4808A>G
ENST00000629765.3:c.1396+4808A>G MANE Select	ENSP00000485864.1:n.1396+4808A>G
ENST00000695462.1:c.1396+4808A>G	ENSP00000511942.1:n.1396+4808A>G
ENST00000695463.1:c.1078+4808A>G	ENSP00000511943.1:n.1078+4808A>G
ENST00000317501.7:c.1396+4808A>G	ENSP00000318328.3:n.1396+4808A>G
ENST00000355254.6:c.1372+4808A>G	ENSP00000347397.3:n.1372+4808A>G
ENST00000357724.6:c.1372+4808A>G	ENSP00000350356.2:n.1372+4808A>G
ENST00000360948.6:c.1396+4808A>G	ENSP00000354207.2:n.1396+4808A>G
ENST00000394480.6:c.1396+4808A>G	ENSP00000377990.1:n.1396+4808A>G
ENST00000540489.6:c.1396+4808A>G	ENSP00000444673.2:n.1396+4808A>G
ENST00000542733.6:c.1102+4808A>G	ENSP00000437773.2:n.1102+4808A>G
ENST00000557856.5:c.1372+4808A>G	ENSP00000453959.1:n.1372+4808A>G
ENST00000557897.1:n.91+4808A>G
ENST00000558306.1:c.30+5699A>G	ENSP00000480693.1:n.30+5699A>G
ENST00000558676.5:c.1372+4808A>G	ENSP00000453511.1:n.1372+4808A>G
ENST00000560017.1:c.208+4808A>G	ENSP00000473475.1:n.208+4808A>G
ENST00000626019.2:c.1396+4808A>G	ENSP00000486784.1:n.1396+4808A>G
ENST00000629765.2:c.1396+4808A>G	ENSP00000485864.1:n.1396+4808A>G
NM_001007156.2:c.1396+4808A>G	NP_001007157.1:n.1396+4808A>G
NM_001012338.2:c.1396+4808A>G	NP_001012338.1:n.1396+4808A>G
NM_001243101.1:c.1372+4808A>G	NP_001230030.1:n.1372+4808A>G
NM_002530.3:c.1396+4808A>G	NP_002521.2:n.1396+4808A>G
XM_006720543.2:c.1396+4808A>G	XP_006720606.1:n.1396+4808A>G
XM_006720544.2:c.1372+4808A>G	XP_006720607.1:n.1372+4808A>G
XM_006720545.2:c.1396+4808A>G	XP_006720608.1:n.1396+4808A>G
XM_006720546.2:c.1396+4808A>G	XP_006720609.1:n.1396+4808A>G
XM_006720547.2:c.1396+4808A>G	XP_006720610.1:n.1396+4808A>G
XM_006720548.2:c.1396+4808A>G	XP_006720611.1:n.1396+4808A>G
XM_006720549.2:c.1396+4808A>G	XP_006720612.1:n.1396+4808A>G
XM_006720550.2:c.1372+4808A>G	XP_006720613.1:n.1372+4808A>G
XM_011521634.1:c.1396+4808A>G	XP_011519936.1:n.1396+4808A>G
XM_011521635.1:c.1396+4808A>G	XP_011519937.1:n.1396+4808A>G
XM_011521636.1:c.1102+4808A>G	XP_011519938.1:n.1102+4808A>G
XM_011521637.1:c.1396+4808A>G	XP_011519939.1:n.1396+4808A>G
XM_011521638.1:c.1396+4808A>G	XP_011519940.1:n.1396+4808A>G
XR_931841.1:n.1435+4808A>G
XR_931842.1:n.1459+4808A>G
NM_001320134.1:c.1396+4808A>G	NP_001307063.1:n.1396+4808A>G
NM_001320135.1:c.1102+4808A>G	NP_001307064.1:n.1102+4808A>G
XM_006720543.4:c.1396+4808A>G	XP_006720606.1:n.1396+4808A>G
XM_006720544.4:c.1372+4808A>G	XP_006720607.1:n.1372+4808A>G
XM_006720545.4:c.1396+4808A>G	XP_006720608.1:n.1396+4808A>G
XM_006720548.4:c.1396+4808A>G	XP_006720611.1:n.1396+4808A>G
XM_006720549.4:c.1396+4808A>G	XP_006720612.1:n.1396+4808A>G
XM_006720550.4:c.1372+4808A>G	XP_006720613.1:n.1372+4808A>G
XM_011521637.3:c.1396+4808A>G	XP_011519939.1:n.1396+4808A>G
XM_011521638.3:c.1396+4808A>G	XP_011519940.1:n.1396+4808A>G
XM_017022240.1:c.1396+4808A>G	XP_016877729.1:n.1396+4808A>G
XM_017022241.1:c.1210+4808A>G	XP_016877730.1:n.1210+4808A>G
XM_017022242.2:c.1396+4808A>G	XP_016877731.1:n.1396+4808A>G
XM_017022243.1:c.1102+4808A>G	XP_016877732.1:n.1102+4808A>G
XM_017022244.2:c.1102+4808A>G	XP_016877733.1:n.1102+4808A>G
XM_017022245.2:c.1102+4808A>G	XP_016877734.1:n.1102+4808A>G
XM_017022247.2:c.1372+4808A>G	XP_016877736.1:n.1372+4808A>G
XM_017022248.2:c.1372+4808A>G	XP_016877737.1:n.1372+4808A>G
XM_017022250.2:c.1396+4808A>G	XP_016877739.1:n.1396+4808A>G
XM_017022251.2:c.289+4808A>G	XP_016877740.1:n.289+4808A>G
XM_017022252.2:c.265+4808A>G	XP_016877741.1:n.265+4808A>G
XM_017022253.2:c.1396+4808A>G	XP_016877742.1:n.1396+4808A>G
XM_017022254.2:c.1396+4808A>G	XP_016877743.1:n.1396+4808A>G
XM_024449933.1:c.1078+4808A>G	XP_024305701.1:n.1078+4808A>G
XM_024449934.1:c.1396+4808A>G	XP_024305702.1:n.1396+4808A>G
XM_024449935.1:c.1396+4808A>G	XP_024305703.1:n.1396+4808A>G
XM_024449936.1:c.1102+4808A>G	XP_024305704.1:n.1102+4808A>G
XR_001751292.2:n.2039+4808A>G
XR_001751293.2:n.2034+4808A>G
XR_002957645.1:n.2011+4808A>G
NM_001375810.1:c.1396+4808A>G	NP_001362739.1:n.1396+4808A>G
NM_001375811.1:c.1396+4808A>G	NP_001362740.1:n.1396+4808A>G
NM_001375812.1:c.1372+4808A>G	NP_001362741.1:n.1372+4808A>G
NM_001375813.1:c.1396+4808A>G	NP_001362742.1:n.1396+4808A>G
NM_001375814.1:c.1372+4808A>G	NP_001362743.1:n.1372+4808A>G
NM_002530.4:c.1396+4808A>G	NP_002521.2:n.1396+4808A>G
NM_001007156.3:c.1396+4808A>G	NP_001007157.1:n.1396+4808A>G
NM_001012338.3:c.1396+4808A>G MANE Select	NP_001012338.1:n.1396+4808A>G
NM_001243101.2:c.1372+4808A>G	NP_001230030.1:n.1372+4808A>G
NM_001320135.2:c.1102+4808A>G	NP_001307064.1:n.1102+4808A>G