Canonical Allele Identifier: CA350708855
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489215A>C , CM000664.2:g.219489215A>C GRCh38
NC_000002.11:g.220353937A>C , CM000664.1:g.220353937A>C GRCh37
NC_000002.10:g.220062181A>C NCBI36
NG_051022.1:g.60001A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8311A>C (SPEG) MANE Select ENSP00000311684.7:p.Thr2771Pro
ENST00000312358.11:c.8311A>C (SPEG) ENSP00000311684.7:p.Thr2771Pro
ENST00000485813.5:n.7554A>C (SPEG)
NM_005876.4:c.8311A>C (SPEG) NP_005867.3:p.Thr2771Pro
XM_005246237.2:c.8029A>C (SPEG) XP_005246294.1:p.Thr2677Pro
XM_005246239.2:c.5935A>C (SPEG) XP_005246296.1:p.Thr1979Pro
XM_005246240.2:c.5764A>C (SPEG) XP_005246297.1:p.Thr1922Pro
XM_005246241.1:c.5764A>C (SPEG) XP_005246298.1:p.Thr1922Pro
XM_005246242.3:c.5950A>C (SPEG) XP_005246299.1:p.Thr1984Pro
XM_006712189.2:c.7999A>C (SPEG) XP_006712252.1:p.Thr2667Pro
XM_006712193.2:c.5764A>C (SPEG) XP_006712256.1:p.Thr1922Pro
XM_011510479.1:c.8341A>C (SPEG) XP_011508781.1:p.Thr2781Pro
XM_011510480.1:c.8173A>C (SPEG) XP_011508782.1:p.Thr2725Pro
XM_011510481.1:c.8164A>C (SPEG) XP_011508783.1:p.Thr2722Pro
XM_011510482.1:c.8158A>C (SPEG) XP_011508784.1:p.Thr2720Pro
XM_011510483.1:c.8080A>C (SPEG) XP_011508785.1:p.Thr2694Pro
XM_011510484.1:c.7996A>C (SPEG) XP_011508786.1:p.Thr2666Pro
XR_923921.1:n.353-6806T>G (ASIC4-AS1)
XM_005246242.4:c.5950A>C (SPEG) XP_005246299.1:p.Thr1984Pro
XM_006712189.3:c.7999A>C (SPEG) XP_006712252.1:p.Thr2667Pro
XM_006712193.3:c.5764A>C (SPEG) XP_006712256.1:p.Thr1922Pro
XM_011510479.2:c.8341A>C (SPEG) XP_011508781.1:p.Thr2781Pro
XM_011510483.2:c.8059A>C (SPEG) XP_011508785.2:p.Thr2687Pro
XM_017003157.1:c.8059A>C (SPEG) XP_016858646.1:p.Thr2687Pro
XM_017003158.2:c.5764A>C (SPEG) XP_016858647.1:p.Thr1922Pro
XM_017003160.1:c.3319A>C (SPEG) XP_016858649.1:p.Thr1107Pro
XR_923921.2:n.392-6806T>G (ASIC4-AS1)
NM_005876.5:c.8311A>C (SPEG) MANE Select NP_005867.3:p.Thr2771Pro