Canonical Allele Identifier: CA2663486590
Gene: SP110 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.230168913_230168914insGTAA , CM000664.2:g.230168913_230168914insGTAA GRCh38
NC_000002.11:g.231033629_231033630insGTAA , CM000664.1:g.231033629_231033630insGTAA GRCh37
NC_000002.10:g.230741873_230741874insGTAA NCBI36
NG_008295.1:g.56199_56200insTACT , LRG_109:g.56199_56200insTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000698099.1:c.*77+134_*77+135insTACT ENSP00000513563.1:n.*77+134_*77+135insTACT
ENST00000698100.1:c.*77+134_*77+135insTACT ENSP00000513564.1:n.*77+134_*77+135insTACT
ENST00000258381.11:c.*211_*212insTACT MANE Select ENSP00000258381.6:n.*211_*212insTACT
ENST00000358662.9:c.*211_*212insTACT ENSP00000351488.4:n.*211_*212insTACT
ENST00000477068.1:n.1105_1106insTACT
XM_005246525.2:c.*211_*212insTACT XP_005246582.1:n.*211_*212insTACT
XM_006712487.2:c.*211_*212insTACT XP_006712550.1:n.*211_*212insTACT
XM_006712489.2:c.*211_*212insTACT XP_006712552.1:n.*211_*212insTACT
XM_011511088.1:c.*211_*212insTACT XP_011509390.1:n.*211_*212insTACT
XM_011511089.1:c.*211_*212insTACT XP_011509391.1:n.*211_*212insTACT
XM_011511090.1:c.*211_*212insTACT XP_011509392.1:n.*211_*212insTACT
XM_011511091.1:c.*211_*212insTACT XP_011509393.1:n.*211_*212insTACT
XM_011511092.1:c.*211_*212insTACT XP_011509394.1:n.*211_*212insTACT
XM_005246525.4:c.*211_*212insTACT XP_005246582.1:n.*211_*212insTACT
XM_006712489.4:c.*211_*212insTACT XP_006712552.1:n.*211_*212insTACT
XM_011511088.3:c.*211_*212insTACT XP_011509390.1:n.*211_*212insTACT
XM_011511091.3:c.*211_*212insTACT XP_011509393.1:n.*211_*212insTACT
XM_024452850.1:c.*211_*212insTACT XP_024308618.1:n.*211_*212insTACT
NM_004509.4:c.*211_*212insTACT NP_004500.4:n.*211_*212insTACT
NM_080424.3:c.*211_*212insTACT NP_536349.3:n.*211_*212insTACT
NM_001378442.1:c.*211_*212insTACT NP_001365371.1:n.*211_*212insTACT
NM_001378443.1:c.*211_*212insTACT NP_001365372.1:n.*211_*212insTACT
NM_001378444.1:c.*211_*212insTACT NP_001365373.1:n.*211_*212insTACT
NM_001378445.1:c.*211_*212insTACT NP_001365374.1:n.*211_*212insTACT
NM_001378446.1:c.*211_*212insTACT NP_001365375.1:n.*211_*212insTACT
NM_004509.5:c.*211_*212insTACT NP_004500.4:n.*211_*212insTACT
NM_080424.4:c.*211_*212insTACT MANE Select NP_536349.3:n.*211_*212insTACT