Canonical Allele Identifier: CA1984826774
Gene: TENM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78708549A= , CM000673.2:g.78708549A= GRCh38
NC_000011.9:g.78419594A= , CM000673.1:g.78419594A= GRCh37
NC_000011.8:g.78097242A= NCBI36
NG_051803.1:g.737103T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278550.12:c.4055-34T= MANE Select ENSP00000278550.7:n.4055-34T=
ENST00000278550.11:c.4055-34T= ENSP00000278550.7:n.4055-34T=
ENST00000612046.4:c.4055-34T= ENSP00000483150.1:n.4055-34T=
NM_001098816.2:c.4055-34T= NP_001092286.2:n.4055-34T=
XM_011544924.1:c.4103-34T= XP_011543226.1:n.4103-34T=
XM_011544925.1:c.4103-34T= XP_011543227.1:n.4103-34T=
XM_011544927.1:c.4082-34T= XP_011543229.1:n.4082-34T=
XM_011544928.1:c.4028-34T= XP_011543230.1:n.4028-34T=
XM_011544929.1:c.4004-34T= XP_011543231.1:n.4004-34T=
XM_011544930.1:c.3899-34T= XP_011543232.1:n.3899-34T=
XM_011544931.1:c.2942-34T= XP_011543233.1:n.2942-34T=
XM_011544932.1:c.1556-34T= XP_011543234.1:n.1556-34T=
XM_011544933.1:c.1499-34T= XP_011543235.1:n.1499-34T=
XM_011544934.1:c.-47-34T= XP_011543236.1:n.-47-34T=
XM_011544933.3:c.1499-34T= XP_011543235.1:n.1499-34T=
XM_017017525.1:c.4130-34T= XP_016873014.1:n.4130-34T=
XM_017017526.1:c.4055-34T= XP_016873015.1:n.4055-34T=
NM_001098816.3:c.4055-34T= MANE Select NP_001092286.2:n.4055-34T=