Canonical Allele Identifier: CA350708808
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489194G>T , CM000664.2:g.219489194G>T GRCh38
NC_000002.11:g.220353916G>T , CM000664.1:g.220353916G>T GRCh37
NC_000002.10:g.220062160G>T NCBI36
NG_051022.1:g.59980G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8290G>T (SPEG) MANE Select ENSP00000311684.7:p.Glu2764Ter
ENST00000312358.11:c.8290G>T (SPEG) ENSP00000311684.7:p.Glu2764Ter
ENST00000485813.5:n.7533G>T (SPEG)
NM_005876.4:c.8290G>T (SPEG) NP_005867.3:p.Glu2764Ter
XM_005246237.2:c.8008G>T (SPEG) XP_005246294.1:p.Glu2670Ter
XM_005246239.2:c.5914G>T (SPEG) XP_005246296.1:p.Glu1972Ter
XM_005246240.2:c.5743G>T (SPEG) XP_005246297.1:p.Glu1915Ter
XM_005246241.1:c.5743G>T (SPEG) XP_005246298.1:p.Glu1915Ter
XM_005246242.3:c.5929G>T (SPEG) XP_005246299.1:p.Glu1977Ter
XM_006712189.2:c.7978G>T (SPEG) XP_006712252.1:p.Glu2660Ter
XM_006712193.2:c.5743G>T (SPEG) XP_006712256.1:p.Glu1915Ter
XM_011510479.1:c.8320G>T (SPEG) XP_011508781.1:p.Glu2774Ter
XM_011510480.1:c.8152G>T (SPEG) XP_011508782.1:p.Glu2718Ter
XM_011510481.1:c.8143G>T (SPEG) XP_011508783.1:p.Glu2715Ter
XM_011510482.1:c.8137G>T (SPEG) XP_011508784.1:p.Glu2713Ter
XM_011510483.1:c.8059G>T (SPEG) XP_011508785.1:p.Glu2687Ter
XM_011510484.1:c.7975G>T (SPEG) XP_011508786.1:p.Glu2659Ter
XR_923921.1:n.353-6785C>A (ASIC4-AS1)
XM_005246242.4:c.5929G>T (SPEG) XP_005246299.1:p.Glu1977Ter
XM_006712189.3:c.7978G>T (SPEG) XP_006712252.1:p.Glu2660Ter
XM_006712193.3:c.5743G>T (SPEG) XP_006712256.1:p.Glu1915Ter
XM_011510479.2:c.8320G>T (SPEG) XP_011508781.1:p.Glu2774Ter
XM_011510483.2:c.8038G>T (SPEG) XP_011508785.2:p.Glu2680Ter
XM_017003157.1:c.8038G>T (SPEG) XP_016858646.1:p.Glu2680Ter
XM_017003158.2:c.5743G>T (SPEG) XP_016858647.1:p.Glu1915Ter
XM_017003160.1:c.3298G>T (SPEG) XP_016858649.1:p.Glu1100Ter
XR_923921.2:n.392-6785C>A (ASIC4-AS1)
NM_005876.5:c.8290G>T (SPEG) MANE Select NP_005867.3:p.Glu2764Ter