Canonical Allele Identifier: CA350708677
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489129T>A , CM000664.2:g.219489129T>A GRCh38
NC_000002.11:g.220353851T>A , CM000664.1:g.220353851T>A GRCh37
NC_000002.10:g.220062095T>A NCBI36
NG_051022.1:g.59915T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8225T>A (SPEG) MANE Select ENSP00000311684.7:p.Val2742Glu
ENST00000312358.11:c.8225T>A (SPEG) ENSP00000311684.7:p.Val2742Glu
ENST00000485813.5:n.7468T>A (SPEG)
NM_005876.4:c.8225T>A (SPEG) NP_005867.3:p.Val2742Glu
XM_005246237.2:c.7943T>A (SPEG) XP_005246294.1:p.Val2648Glu
XM_005246239.2:c.5849T>A (SPEG) XP_005246296.1:p.Val1950Glu
XM_005246240.2:c.5678T>A (SPEG) XP_005246297.1:p.Val1893Glu
XM_005246241.1:c.5678T>A (SPEG) XP_005246298.1:p.Val1893Glu
XM_005246242.3:c.5864T>A (SPEG) XP_005246299.1:p.Val1955Glu
XM_006712189.2:c.7913T>A (SPEG) XP_006712252.1:p.Val2638Glu
XM_006712193.2:c.5678T>A (SPEG) XP_006712256.1:p.Val1893Glu
XM_011510479.1:c.8255T>A (SPEG) XP_011508781.1:p.Val2752Glu
XM_011510480.1:c.8087T>A (SPEG) XP_011508782.1:p.Val2696Glu
XM_011510481.1:c.8078T>A (SPEG) XP_011508783.1:p.Val2693Glu
XM_011510482.1:c.8072T>A (SPEG) XP_011508784.1:p.Val2691Glu
XM_011510483.1:c.7994T>A (SPEG) XP_011508785.1:p.Val2665Glu
XM_011510484.1:c.7910T>A (SPEG) XP_011508786.1:p.Val2637Glu
XR_923921.1:n.353-6720A>T (ASIC4-AS1)
XM_005246242.4:c.5864T>A (SPEG) XP_005246299.1:p.Val1955Glu
XM_006712189.3:c.7913T>A (SPEG) XP_006712252.1:p.Val2638Glu
XM_006712193.3:c.5678T>A (SPEG) XP_006712256.1:p.Val1893Glu
XM_011510479.2:c.8255T>A (SPEG) XP_011508781.1:p.Val2752Glu
XM_011510483.2:c.7973T>A (SPEG) XP_011508785.2:p.Val2658Glu
XM_017003157.1:c.7973T>A (SPEG) XP_016858646.1:p.Val2658Glu
XM_017003158.2:c.5678T>A (SPEG) XP_016858647.1:p.Val1893Glu
XM_017003160.1:c.3233T>A (SPEG) XP_016858649.1:p.Val1078Glu
XR_923921.2:n.392-6720A>T (ASIC4-AS1)
NM_005876.5:c.8225T>A (SPEG) MANE Select NP_005867.3:p.Val2742Glu