Canonical Allele Identifier: CA350708842
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489207T>G , CM000664.2:g.219489207T>G GRCh38
NC_000002.11:g.220353929T>G , CM000664.1:g.220353929T>G GRCh37
NC_000002.10:g.220062173T>G NCBI36
NG_051022.1:g.59993T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8303T>G (SPEG) MANE Select ENSP00000311684.7:p.Val2768Gly
ENST00000312358.11:c.8303T>G (SPEG) ENSP00000311684.7:p.Val2768Gly
ENST00000485813.5:n.7546T>G (SPEG)
NM_005876.4:c.8303T>G (SPEG) NP_005867.3:p.Val2768Gly
XM_005246237.2:c.8021T>G (SPEG) XP_005246294.1:p.Val2674Gly
XM_005246239.2:c.5927T>G (SPEG) XP_005246296.1:p.Val1976Gly
XM_005246240.2:c.5756T>G (SPEG) XP_005246297.1:p.Val1919Gly
XM_005246241.1:c.5756T>G (SPEG) XP_005246298.1:p.Val1919Gly
XM_005246242.3:c.5942T>G (SPEG) XP_005246299.1:p.Val1981Gly
XM_006712189.2:c.7991T>G (SPEG) XP_006712252.1:p.Val2664Gly
XM_006712193.2:c.5756T>G (SPEG) XP_006712256.1:p.Val1919Gly
XM_011510479.1:c.8333T>G (SPEG) XP_011508781.1:p.Val2778Gly
XM_011510480.1:c.8165T>G (SPEG) XP_011508782.1:p.Val2722Gly
XM_011510481.1:c.8156T>G (SPEG) XP_011508783.1:p.Val2719Gly
XM_011510482.1:c.8150T>G (SPEG) XP_011508784.1:p.Val2717Gly
XM_011510483.1:c.8072T>G (SPEG) XP_011508785.1:p.Val2691Gly
XM_011510484.1:c.7988T>G (SPEG) XP_011508786.1:p.Val2663Gly
XR_923921.1:n.353-6798A>C (ASIC4-AS1)
XM_005246242.4:c.5942T>G (SPEG) XP_005246299.1:p.Val1981Gly
XM_006712189.3:c.7991T>G (SPEG) XP_006712252.1:p.Val2664Gly
XM_006712193.3:c.5756T>G (SPEG) XP_006712256.1:p.Val1919Gly
XM_011510479.2:c.8333T>G (SPEG) XP_011508781.1:p.Val2778Gly
XM_011510483.2:c.8051T>G (SPEG) XP_011508785.2:p.Val2684Gly
XM_017003157.1:c.8051T>G (SPEG) XP_016858646.1:p.Val2684Gly
XM_017003158.2:c.5756T>G (SPEG) XP_016858647.1:p.Val1919Gly
XM_017003160.1:c.3311T>G (SPEG) XP_016858649.1:p.Val1104Gly
XR_923921.2:n.392-6798A>C (ASIC4-AS1)
NM_005876.5:c.8303T>G (SPEG) MANE Select NP_005867.3:p.Val2768Gly