Canonical Allele Identifier: CA350708843
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489209A>G , CM000664.2:g.219489209A>G GRCh38
NC_000002.11:g.220353931A>G , CM000664.1:g.220353931A>G GRCh37
NC_000002.10:g.220062175A>G NCBI36
NG_051022.1:g.59995A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8305A>G (SPEG) MANE Select ENSP00000311684.7:p.Arg2769Gly
ENST00000312358.11:c.8305A>G (SPEG) ENSP00000311684.7:p.Arg2769Gly
ENST00000485813.5:n.7548A>G (SPEG)
NM_005876.4:c.8305A>G (SPEG) NP_005867.3:p.Arg2769Gly
XM_005246237.2:c.8023A>G (SPEG) XP_005246294.1:p.Arg2675Gly
XM_005246239.2:c.5929A>G (SPEG) XP_005246296.1:p.Arg1977Gly
XM_005246240.2:c.5758A>G (SPEG) XP_005246297.1:p.Arg1920Gly
XM_005246241.1:c.5758A>G (SPEG) XP_005246298.1:p.Arg1920Gly
XM_005246242.3:c.5944A>G (SPEG) XP_005246299.1:p.Arg1982Gly
XM_006712189.2:c.7993A>G (SPEG) XP_006712252.1:p.Arg2665Gly
XM_006712193.2:c.5758A>G (SPEG) XP_006712256.1:p.Arg1920Gly
XM_011510479.1:c.8335A>G (SPEG) XP_011508781.1:p.Arg2779Gly
XM_011510480.1:c.8167A>G (SPEG) XP_011508782.1:p.Arg2723Gly
XM_011510481.1:c.8158A>G (SPEG) XP_011508783.1:p.Arg2720Gly
XM_011510482.1:c.8152A>G (SPEG) XP_011508784.1:p.Arg2718Gly
XM_011510483.1:c.8074A>G (SPEG) XP_011508785.1:p.Arg2692Gly
XM_011510484.1:c.7990A>G (SPEG) XP_011508786.1:p.Arg2664Gly
XR_923921.1:n.353-6800T>C (ASIC4-AS1)
XM_005246242.4:c.5944A>G (SPEG) XP_005246299.1:p.Arg1982Gly
XM_006712189.3:c.7993A>G (SPEG) XP_006712252.1:p.Arg2665Gly
XM_006712193.3:c.5758A>G (SPEG) XP_006712256.1:p.Arg1920Gly
XM_011510479.2:c.8335A>G (SPEG) XP_011508781.1:p.Arg2779Gly
XM_011510483.2:c.8053A>G (SPEG) XP_011508785.2:p.Arg2685Gly
XM_017003157.1:c.8053A>G (SPEG) XP_016858646.1:p.Arg2685Gly
XM_017003158.2:c.5758A>G (SPEG) XP_016858647.1:p.Arg1920Gly
XM_017003160.1:c.3313A>G (SPEG) XP_016858649.1:p.Arg1105Gly
XR_923921.2:n.392-6800T>C (ASIC4-AS1)
NM_005876.5:c.8305A>G (SPEG) MANE Select NP_005867.3:p.Arg2769Gly