Canonical Allele Identifier: CA350708851
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489212G>C , CM000664.2:g.219489212G>C GRCh38
NC_000002.11:g.220353934G>C , CM000664.1:g.220353934G>C GRCh37
NC_000002.10:g.220062178G>C NCBI36
NG_051022.1:g.59998G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8308G>C (SPEG) MANE Select ENSP00000311684.7:p.Gly2770Arg
ENST00000312358.11:c.8308G>C (SPEG) ENSP00000311684.7:p.Gly2770Arg
ENST00000485813.5:n.7551G>C (SPEG)
NM_005876.4:c.8308G>C (SPEG) NP_005867.3:p.Gly2770Arg
XM_005246237.2:c.8026G>C (SPEG) XP_005246294.1:p.Gly2676Arg
XM_005246239.2:c.5932G>C (SPEG) XP_005246296.1:p.Gly1978Arg
XM_005246240.2:c.5761G>C (SPEG) XP_005246297.1:p.Gly1921Arg
XM_005246241.1:c.5761G>C (SPEG) XP_005246298.1:p.Gly1921Arg
XM_005246242.3:c.5947G>C (SPEG) XP_005246299.1:p.Gly1983Arg
XM_006712189.2:c.7996G>C (SPEG) XP_006712252.1:p.Gly2666Arg
XM_006712193.2:c.5761G>C (SPEG) XP_006712256.1:p.Gly1921Arg
XM_011510479.1:c.8338G>C (SPEG) XP_011508781.1:p.Gly2780Arg
XM_011510480.1:c.8170G>C (SPEG) XP_011508782.1:p.Gly2724Arg
XM_011510481.1:c.8161G>C (SPEG) XP_011508783.1:p.Gly2721Arg
XM_011510482.1:c.8155G>C (SPEG) XP_011508784.1:p.Gly2719Arg
XM_011510483.1:c.8077G>C (SPEG) XP_011508785.1:p.Gly2693Arg
XM_011510484.1:c.7993G>C (SPEG) XP_011508786.1:p.Gly2665Arg
XR_923921.1:n.353-6803C>G (ASIC4-AS1)
XM_005246242.4:c.5947G>C (SPEG) XP_005246299.1:p.Gly1983Arg
XM_006712189.3:c.7996G>C (SPEG) XP_006712252.1:p.Gly2666Arg
XM_006712193.3:c.5761G>C (SPEG) XP_006712256.1:p.Gly1921Arg
XM_011510479.2:c.8338G>C (SPEG) XP_011508781.1:p.Gly2780Arg
XM_011510483.2:c.8056G>C (SPEG) XP_011508785.2:p.Gly2686Arg
XM_017003157.1:c.8056G>C (SPEG) XP_016858646.1:p.Gly2686Arg
XM_017003158.2:c.5761G>C (SPEG) XP_016858647.1:p.Gly1921Arg
XM_017003160.1:c.3316G>C (SPEG) XP_016858649.1:p.Gly1106Arg
XR_923921.2:n.392-6803C>G (ASIC4-AS1)
NM_005876.5:c.8308G>C (SPEG) MANE Select NP_005867.3:p.Gly2770Arg