Canonical Allele Identifier: CA350708862
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489218C>T , CM000664.2:g.219489218C>T GRCh38
NC_000002.11:g.220353940C>T , CM000664.1:g.220353940C>T GRCh37
NC_000002.10:g.220062184C>T NCBI36
NG_051022.1:g.60004C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8314C>T (SPEG) MANE Select ENSP00000311684.7:p.Gln2772Ter
ENST00000312358.11:c.8314C>T (SPEG) ENSP00000311684.7:p.Gln2772Ter
ENST00000485813.5:n.7557C>T (SPEG)
NM_005876.4:c.8314C>T (SPEG) NP_005867.3:p.Gln2772Ter
XM_005246237.2:c.8032C>T (SPEG) XP_005246294.1:p.Gln2678Ter
XM_005246239.2:c.5938C>T (SPEG) XP_005246296.1:p.Gln1980Ter
XM_005246240.2:c.5767C>T (SPEG) XP_005246297.1:p.Gln1923Ter
XM_005246241.1:c.5767C>T (SPEG) XP_005246298.1:p.Gln1923Ter
XM_005246242.3:c.5953C>T (SPEG) XP_005246299.1:p.Gln1985Ter
XM_006712189.2:c.8002C>T (SPEG) XP_006712252.1:p.Gln2668Ter
XM_006712193.2:c.5767C>T (SPEG) XP_006712256.1:p.Gln1923Ter
XM_011510479.1:c.8344C>T (SPEG) XP_011508781.1:p.Gln2782Ter
XM_011510480.1:c.8176C>T (SPEG) XP_011508782.1:p.Gln2726Ter
XM_011510481.1:c.8167C>T (SPEG) XP_011508783.1:p.Gln2723Ter
XM_011510482.1:c.8161C>T (SPEG) XP_011508784.1:p.Gln2721Ter
XM_011510483.1:c.8083C>T (SPEG) XP_011508785.1:p.Gln2695Ter
XM_011510484.1:c.7999C>T (SPEG) XP_011508786.1:p.Gln2667Ter
XR_923921.1:n.353-6809G>A (ASIC4-AS1)
XM_005246242.4:c.5953C>T (SPEG) XP_005246299.1:p.Gln1985Ter
XM_006712189.3:c.8002C>T (SPEG) XP_006712252.1:p.Gln2668Ter
XM_006712193.3:c.5767C>T (SPEG) XP_006712256.1:p.Gln1923Ter
XM_011510479.2:c.8344C>T (SPEG) XP_011508781.1:p.Gln2782Ter
XM_011510483.2:c.8062C>T (SPEG) XP_011508785.2:p.Gln2688Ter
XM_017003157.1:c.8062C>T (SPEG) XP_016858646.1:p.Gln2688Ter
XM_017003158.2:c.5767C>T (SPEG) XP_016858647.1:p.Gln1923Ter
XM_017003160.1:c.3322C>T (SPEG) XP_016858649.1:p.Gln1108Ter
XR_923921.2:n.392-6809G>A (ASIC4-AS1)
NM_005876.5:c.8314C>T (SPEG) MANE Select NP_005867.3:p.Gln2772Ter