Canonical Allele Identifier: CA6206076
Gene: TENM4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3175969
ClinVar RCV Id: RCV004469778
dbSNP Id: rs779399051

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78658216G>A , CM000673.2:g.78658216G>A GRCh38
NC_000011.9:g.78369261G>A , CM000673.1:g.78369261G>A GRCh37
NC_000011.8:g.78046909G>A NCBI36
NG_051803.1:g.787436C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278550.12:c.8152C>T MANE Select ENSP00000278550.7:p.Arg2718Trp
ENST00000278550.11:c.8152C>T ENSP00000278550.7:p.Arg2718Trp
ENST00000530738.1:c.2801-162C>T ENSP00000431711.1:n.2801-162C>T
ENST00000612046.4:c.8152C>T ENSP00000483150.1:p.Arg2718Trp
NM_001098816.2:c.8152C>T NP_001092286.2:p.Arg2718Trp
XM_011544924.1:c.8200C>T XP_011543226.1:p.Arg2734Trp
XM_011544925.1:c.8200C>T XP_011543227.1:p.Arg2734Trp
XM_011544927.1:c.8179C>T XP_011543229.1:p.Arg2727Trp
XM_011544928.1:c.8125C>T XP_011543230.1:p.Arg2709Trp
XM_011544929.1:c.8101C>T XP_011543231.1:p.Arg2701Trp
XM_011544930.1:c.7996C>T XP_011543232.1:p.Arg2666Trp
XM_011544931.1:c.7039C>T XP_011543233.1:p.Arg2347Trp
XM_011544932.1:c.5653C>T XP_011543234.1:p.Arg1885Trp
XM_011544933.1:c.5596C>T XP_011543235.1:p.Arg1866Trp
XM_011544934.1:c.4051C>T XP_011543236.1:p.Arg1351Trp
XM_011544933.3:c.5596C>T XP_011543235.1:p.Arg1866Trp
XM_017017525.1:c.8227C>T XP_016873014.1:p.Arg2743Trp
XM_017017526.1:c.8152C>T XP_016873015.1:p.Arg2718Trp
NM_001098816.3:c.8152C>T MANE Select NP_001092286.2:p.Arg2718Trp