Canonical Allele Identifier: CA350708788
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489184C>G , CM000664.2:g.219489184C>G GRCh38
NC_000002.11:g.220353906C>G , CM000664.1:g.220353906C>G GRCh37
NC_000002.10:g.220062150C>G NCBI36
NG_051022.1:g.59970C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8280C>G (SPEG) MANE Select ENSP00000311684.7:p.Ser2760Arg
ENST00000312358.11:c.8280C>G (SPEG) ENSP00000311684.7:p.Ser2760Arg
ENST00000485813.5:n.7523C>G (SPEG)
NM_005876.4:c.8280C>G (SPEG) NP_005867.3:p.Ser2760Arg
XM_005246237.2:c.7998C>G (SPEG) XP_005246294.1:p.Ser2666Arg
XM_005246239.2:c.5904C>G (SPEG) XP_005246296.1:p.Ser1968Arg
XM_005246240.2:c.5733C>G (SPEG) XP_005246297.1:p.Ser1911Arg
XM_005246241.1:c.5733C>G (SPEG) XP_005246298.1:p.Ser1911Arg
XM_005246242.3:c.5919C>G (SPEG) XP_005246299.1:p.Ser1973Arg
XM_006712189.2:c.7968C>G (SPEG) XP_006712252.1:p.Ser2656Arg
XM_006712193.2:c.5733C>G (SPEG) XP_006712256.1:p.Ser1911Arg
XM_011510479.1:c.8310C>G (SPEG) XP_011508781.1:p.Ser2770Arg
XM_011510480.1:c.8142C>G (SPEG) XP_011508782.1:p.Ser2714Arg
XM_011510481.1:c.8133C>G (SPEG) XP_011508783.1:p.Ser2711Arg
XM_011510482.1:c.8127C>G (SPEG) XP_011508784.1:p.Ser2709Arg
XM_011510483.1:c.8049C>G (SPEG) XP_011508785.1:p.Ser2683Arg
XM_011510484.1:c.7965C>G (SPEG) XP_011508786.1:p.Ser2655Arg
XR_923921.1:n.353-6775G>C (ASIC4-AS1)
XM_005246242.4:c.5919C>G (SPEG) XP_005246299.1:p.Ser1973Arg
XM_006712189.3:c.7968C>G (SPEG) XP_006712252.1:p.Ser2656Arg
XM_006712193.3:c.5733C>G (SPEG) XP_006712256.1:p.Ser1911Arg
XM_011510479.2:c.8310C>G (SPEG) XP_011508781.1:p.Ser2770Arg
XM_011510483.2:c.8028C>G (SPEG) XP_011508785.2:p.Ser2676Arg
XM_017003157.1:c.8028C>G (SPEG) XP_016858646.1:p.Ser2676Arg
XM_017003158.2:c.5733C>G (SPEG) XP_016858647.1:p.Ser1911Arg
XM_017003160.1:c.3288C>G (SPEG) XP_016858649.1:p.Ser1096Arg
XR_923921.2:n.392-6775G>C (ASIC4-AS1)
NM_005876.5:c.8280C>G (SPEG) MANE Select NP_005867.3:p.Ser2760Arg