Canonical Allele Identifier: CA350708579
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489083G>A , CM000664.2:g.219489083G>A GRCh38
NC_000002.11:g.220353805G>A , CM000664.1:g.220353805G>A GRCh37
NC_000002.10:g.220062049G>A NCBI36
NG_051022.1:g.59869G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8179G>A (SPEG) MANE Select ENSP00000311684.7:p.Gly2727Ser
ENST00000312358.11:c.8179G>A (SPEG) ENSP00000311684.7:p.Gly2727Ser
ENST00000485813.5:n.7422G>A (SPEG)
NM_005876.4:c.8179G>A (SPEG) NP_005867.3:p.Gly2727Ser
XM_005246237.2:c.7897G>A (SPEG) XP_005246294.1:p.Gly2633Ser
XM_005246239.2:c.5803G>A (SPEG) XP_005246296.1:p.Gly1935Ser
XM_005246240.2:c.5632G>A (SPEG) XP_005246297.1:p.Gly1878Ser
XM_005246241.1:c.5632G>A (SPEG) XP_005246298.1:p.Gly1878Ser
XM_005246242.3:c.5818G>A (SPEG) XP_005246299.1:p.Gly1940Ser
XM_006712189.2:c.7867G>A (SPEG) XP_006712252.1:p.Gly2623Ser
XM_006712193.2:c.5632G>A (SPEG) XP_006712256.1:p.Gly1878Ser
XM_011510479.1:c.8209G>A (SPEG) XP_011508781.1:p.Gly2737Ser
XM_011510480.1:c.8041G>A (SPEG) XP_011508782.1:p.Gly2681Ser
XM_011510481.1:c.8032G>A (SPEG) XP_011508783.1:p.Gly2678Ser
XM_011510482.1:c.8026G>A (SPEG) XP_011508784.1:p.Gly2676Ser
XM_011510483.1:c.7948G>A (SPEG) XP_011508785.1:p.Gly2650Ser
XM_011510484.1:c.7864G>A (SPEG) XP_011508786.1:p.Gly2622Ser
XR_923921.1:n.353-6674C>T (ASIC4-AS1)
XM_005246242.4:c.5818G>A (SPEG) XP_005246299.1:p.Gly1940Ser
XM_006712189.3:c.7867G>A (SPEG) XP_006712252.1:p.Gly2623Ser
XM_006712193.3:c.5632G>A (SPEG) XP_006712256.1:p.Gly1878Ser
XM_011510479.2:c.8209G>A (SPEG) XP_011508781.1:p.Gly2737Ser
XM_011510483.2:c.7927G>A (SPEG) XP_011508785.2:p.Gly2643Ser
XM_017003157.1:c.7927G>A (SPEG) XP_016858646.1:p.Gly2643Ser
XM_017003158.2:c.5632G>A (SPEG) XP_016858647.1:p.Gly1878Ser
XM_017003160.1:c.3187G>A (SPEG) XP_016858649.1:p.Gly1063Ser
XR_923921.2:n.392-6674C>T (ASIC4-AS1)
NM_005876.5:c.8179G>A (SPEG) MANE Select NP_005867.3:p.Gly2727Ser