Canonical Allele Identifier: CA225141199
Gene: TENM4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.78948100A>T , CM000673.2:g.78948100A>T GRCh38
NC_000011.9:g.78659145A>T , CM000673.1:g.78659145A>T GRCh37
NC_000011.8:g.78336793A>T NCBI36
NG_051803.1:g.497552T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278550.12:c.494-44577T>A MANE Select ENSP00000278550.7:n.494-44577T>A
ENST00000278550.11:c.494-44577T>A ENSP00000278550.7:n.494-44577T>A
ENST00000529798.1:n.400-23354T>A
ENST00000533013.1:n.77+14043T>A
ENST00000612046.4:c.494-44577T>A ENSP00000483150.1:n.494-44577T>A
NM_001098816.2:c.494-44577T>A NP_001092286.2:n.494-44577T>A
XM_011544924.1:c.569-44577T>A XP_011543226.1:n.569-44577T>A
XM_011544925.1:c.569-44577T>A XP_011543227.1:n.569-44577T>A
XM_011544927.1:c.569-44577T>A XP_011543229.1:n.569-44577T>A
XM_011544928.1:c.494-44577T>A XP_011543230.1:n.494-44577T>A
XM_011544929.1:c.569-44577T>A XP_011543231.1:n.569-44577T>A
XM_011544930.1:c.364+14043T>A XP_011543232.1:n.364+14043T>A
XM_017017525.1:c.569-44577T>A XP_016873014.1:n.569-44577T>A
XM_017017526.1:c.494-44577T>A XP_016873015.1:n.494-44577T>A
NM_001098816.3:c.494-44577T>A MANE Select NP_001092286.2:n.494-44577T>A
Search 100 bp 5'
Search 100 bp 3'