Canonical Allele Identifier: CA14123970

Gene: NTRK3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87876193T>G , CM000677.2:g.87876193T>G	GRCh38
NC_000015.9:g.88419424T>G , CM000677.1:g.88419424T>G	GRCh37
NC_000015.8:g.86220428T>G	NCBI36
NG_029619.1:g.385539A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000629765.3:c.*742A>C MANE Select	ENSP00000485864.1:n.*742A>C
ENST00000394480.6:c.*742A>C	ENSP00000377990.1:n.*742A>C
XM_006720543.2:c.*742A>C	XP_006720606.1:n.*742A>C
XM_006720544.2:c.*742A>C	XP_006720607.1:n.*742A>C
XM_011521634.1:c.*742A>C	XP_011519936.1:n.*742A>C
XM_011521635.1:c.*742A>C	XP_011519937.1:n.*742A>C
XM_006720543.4:c.*742A>C	XP_006720606.1:n.*742A>C
XM_006720544.4:c.*742A>C	XP_006720607.1:n.*742A>C
XM_017022240.1:c.*742A>C	XP_016877729.1:n.*742A>C
XM_017022241.1:c.*742A>C	XP_016877730.1:n.*742A>C
XM_017022243.1:c.*742A>C	XP_016877732.1:n.*742A>C
XM_017022244.2:c.*742A>C	XP_016877733.1:n.*742A>C
XM_017022245.2:c.*742A>C	XP_016877734.1:n.*742A>C
XM_017022251.2:c.*742A>C	XP_016877740.1:n.*742A>C
XM_017022252.2:c.*742A>C	XP_016877741.1:n.*742A>C
XM_017022253.2:c.*742A>C	XP_016877742.1:n.*742A>C
XM_017022254.2:c.*742A>C	XP_016877743.1:n.*742A>C
XM_024449933.1:c.*742A>C	XP_024305701.1:n.*742A>C
XR_001751292.2:n.3863A>C
NM_001375810.1:c.*742A>C	NP_001362739.1:n.*742A>C
NM_001375811.1:c.*742A>C	NP_001362740.1:n.*742A>C
NM_001375812.1:c.*742A>C	NP_001362741.1:n.*742A>C
NM_002530.4:c.*742A>C	NP_002521.2:n.*742A>C
NM_001012338.3:c.*742A>C MANE Select	NP_001012338.1:n.*742A>C
NM_001243101.2:c.*742A>C	NP_001230030.1:n.*742A>C