Canonical Allele Identifier: CA350708763
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489173G>A , CM000664.2:g.219489173G>A GRCh38
NC_000002.11:g.220353895G>A , CM000664.1:g.220353895G>A GRCh37
NC_000002.10:g.220062139G>A NCBI36
NG_051022.1:g.59959G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8269G>A (SPEG) MANE Select ENSP00000311684.7:p.Gly2757Arg
ENST00000312358.11:c.8269G>A (SPEG) ENSP00000311684.7:p.Gly2757Arg
ENST00000485813.5:n.7512G>A (SPEG)
NM_005876.4:c.8269G>A (SPEG) NP_005867.3:p.Gly2757Arg
XM_005246237.2:c.7987G>A (SPEG) XP_005246294.1:p.Gly2663Arg
XM_005246239.2:c.5893G>A (SPEG) XP_005246296.1:p.Gly1965Arg
XM_005246240.2:c.5722G>A (SPEG) XP_005246297.1:p.Gly1908Arg
XM_005246241.1:c.5722G>A (SPEG) XP_005246298.1:p.Gly1908Arg
XM_005246242.3:c.5908G>A (SPEG) XP_005246299.1:p.Gly1970Arg
XM_006712189.2:c.7957G>A (SPEG) XP_006712252.1:p.Gly2653Arg
XM_006712193.2:c.5722G>A (SPEG) XP_006712256.1:p.Gly1908Arg
XM_011510479.1:c.8299G>A (SPEG) XP_011508781.1:p.Gly2767Arg
XM_011510480.1:c.8131G>A (SPEG) XP_011508782.1:p.Gly2711Arg
XM_011510481.1:c.8122G>A (SPEG) XP_011508783.1:p.Gly2708Arg
XM_011510482.1:c.8116G>A (SPEG) XP_011508784.1:p.Gly2706Arg
XM_011510483.1:c.8038G>A (SPEG) XP_011508785.1:p.Gly2680Arg
XM_011510484.1:c.7954G>A (SPEG) XP_011508786.1:p.Gly2652Arg
XR_923921.1:n.353-6764C>T (ASIC4-AS1)
XM_005246242.4:c.5908G>A (SPEG) XP_005246299.1:p.Gly1970Arg
XM_006712189.3:c.7957G>A (SPEG) XP_006712252.1:p.Gly2653Arg
XM_006712193.3:c.5722G>A (SPEG) XP_006712256.1:p.Gly1908Arg
XM_011510479.2:c.8299G>A (SPEG) XP_011508781.1:p.Gly2767Arg
XM_011510483.2:c.8017G>A (SPEG) XP_011508785.2:p.Gly2673Arg
XM_017003157.1:c.8017G>A (SPEG) XP_016858646.1:p.Gly2673Arg
XM_017003158.2:c.5722G>A (SPEG) XP_016858647.1:p.Gly1908Arg
XM_017003160.1:c.3277G>A (SPEG) XP_016858649.1:p.Gly1093Arg
XR_923921.2:n.392-6764C>T (ASIC4-AS1)
NM_005876.5:c.8269G>A (SPEG) MANE Select NP_005867.3:p.Gly2757Arg