Canonical Allele Identifier: CA275079743

Gene: NTRK3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87876836C>T , CM000677.2:g.87876836C>T	GRCh38
NC_000015.9:g.88420067C>T , CM000677.1:g.88420067C>T	GRCh37
NC_000015.8:g.86221071C>T	NCBI36
NG_029619.1:g.384896G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001012338.3:c.*99G>A MANE Select	NP_001012338.1:n.*99G>A
ENST00000629765.3:c.*99G>A MANE Select	ENSP00000485864.1:n.*99G>A
NM_001012338.2:c.*99G>A	NP_001012338.1:n.*99G>A
NM_001243101.1:c.*99G>A	NP_001230030.1:n.*99G>A
NM_001243101.2:c.*99G>A	NP_001230030.1:n.*99G>A
NM_001375810.1:c.*99G>A	NP_001362739.1:n.*99G>A
NM_001375811.1:c.*99G>A	NP_001362740.1:n.*99G>A
NM_001375812.1:c.*99G>A	NP_001362741.1:n.*99G>A
NM_002530.3:c.*99G>A	NP_002521.2:n.*99G>A
NM_002530.4:c.*99G>A	NP_002521.2:n.*99G>A
ENST00000355254.6:c.*99G>A	ENSP00000347397.3:n.*99G>A
ENST00000357724.6:c.*99G>A	ENSP00000350356.2:n.*99G>A
ENST00000360948.6:c.*99G>A	ENSP00000354207.2:n.*99G>A
ENST00000394480.6:c.*99G>A	ENSP00000377990.1:n.*99G>A
ENST00000557856.5:c.*99G>A	ENSP00000453959.1:n.*99G>A
ENST00000626019.2:c.2694G>A	ENSP00000486784.1:n.2694G>A
ENST00000629765.2:c.*99G>A	ENSP00000485864.1:n.*99G>A
ENST00000695462.1:c.*99G>A	ENSP00000511942.1:n.*99G>A
XM_006720543.2:c.*99G>A	XP_006720606.1:n.*99G>A
XM_006720543.4:c.*99G>A	XP_006720606.1:n.*99G>A
XM_006720544.2:c.*99G>A	XP_006720607.1:n.*99G>A
XM_006720544.4:c.*99G>A	XP_006720607.1:n.*99G>A
XM_011521634.1:c.*99G>A	XP_011519936.1:n.*99G>A
XM_011521635.1:c.*99G>A	XP_011519937.1:n.*99G>A
XM_017022240.1:c.*99G>A	XP_016877729.1:n.*99G>A
XM_017022241.1:c.*99G>A	XP_016877730.1:n.*99G>A
XM_017022243.1:c.*99G>A	XP_016877732.1:n.*99G>A
XM_017022244.2:c.*99G>A	XP_016877733.1:n.*99G>A
XM_017022245.2:c.*99G>A	XP_016877734.1:n.*99G>A
XM_017022251.2:c.*99G>A	XP_016877740.1:n.*99G>A
XM_017022252.2:c.*99G>A	XP_016877741.1:n.*99G>A
XM_017022253.2:c.*99G>A	XP_016877742.1:n.*99G>A
XM_017022254.2:c.*99G>A	XP_016877743.1:n.*99G>A
XM_024449933.1:c.*99G>A	XP_024305701.1:n.*99G>A
XR_001751292.2:n.3220G>A