Canonical Allele Identifier: CA716796157

Gene: NTRK3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.87868912G>C , CM000677.2:g.87868912G>C	GRCh38
NC_000015.9:g.88412143G>C , CM000677.1:g.88412143G>C	GRCh37
NC_000015.8:g.86213147G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000629765.3:c.*8023C>G MANE Select	ENSP00000485864.1:n.*8023C>G
ENST00000394480.6:c.*8023C>G	ENSP00000377990.1:n.*8023C>G
XM_006720543.4:c.*8023C>G	XP_006720606.1:n.*8023C>G
XM_006720544.4:c.*8023C>G	XP_006720607.1:n.*8023C>G
XM_017022240.1:c.*8023C>G	XP_016877729.1:n.*8023C>G
XM_017022241.1:c.*8023C>G	XP_016877730.1:n.*8023C>G
XM_017022243.1:c.*8023C>G	XP_016877732.1:n.*8023C>G
XM_017022244.2:c.*8023C>G	XP_016877733.1:n.*8023C>G
XM_017022245.2:c.*8023C>G	XP_016877734.1:n.*8023C>G
XM_017022251.2:c.*8023C>G	XP_016877740.1:n.*8023C>G
XM_017022252.2:c.*8023C>G	XP_016877741.1:n.*8023C>G
XM_017022253.2:c.*8023C>G	XP_016877742.1:n.*8023C>G
XM_017022254.2:c.*8023C>G	XP_016877743.1:n.*8023C>G
XM_024449933.1:c.*8023C>G	XP_024305701.1:n.*8023C>G
XR_001751292.2:n.11144C>G
NM_001375810.1:c.*8023C>G	NP_001362739.1:n.*8023C>G
NM_001375811.1:c.*8023C>G	NP_001362740.1:n.*8023C>G
NM_001375812.1:c.*8023C>G	NP_001362741.1:n.*8023C>G
NM_002530.4:c.*8023C>G	NP_002521.2:n.*8023C>G
NM_001012338.3:c.*8023C>G MANE Select	NP_001012338.1:n.*8023C>G
NM_001243101.2:c.*8023C>G	NP_001230030.1:n.*8023C>G