Canonical Allele Identifier: CA350708864
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489219A>G , CM000664.2:g.219489219A>G GRCh38
NC_000002.11:g.220353941A>G , CM000664.1:g.220353941A>G GRCh37
NC_000002.10:g.220062185A>G NCBI36
NG_051022.1:g.60005A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8315A>G (SPEG) MANE Select ENSP00000311684.7:p.Gln2772Arg
ENST00000312358.11:c.8315A>G (SPEG) ENSP00000311684.7:p.Gln2772Arg
ENST00000485813.5:n.7558A>G (SPEG)
NM_005876.4:c.8315A>G (SPEG) NP_005867.3:p.Gln2772Arg
XM_005246237.2:c.8033A>G (SPEG) XP_005246294.1:p.Gln2678Arg
XM_005246239.2:c.5939A>G (SPEG) XP_005246296.1:p.Gln1980Arg
XM_005246240.2:c.5768A>G (SPEG) XP_005246297.1:p.Gln1923Arg
XM_005246241.1:c.5768A>G (SPEG) XP_005246298.1:p.Gln1923Arg
XM_005246242.3:c.5954A>G (SPEG) XP_005246299.1:p.Gln1985Arg
XM_006712189.2:c.8003A>G (SPEG) XP_006712252.1:p.Gln2668Arg
XM_006712193.2:c.5768A>G (SPEG) XP_006712256.1:p.Gln1923Arg
XM_011510479.1:c.8345A>G (SPEG) XP_011508781.1:p.Gln2782Arg
XM_011510480.1:c.8177A>G (SPEG) XP_011508782.1:p.Gln2726Arg
XM_011510481.1:c.8168A>G (SPEG) XP_011508783.1:p.Gln2723Arg
XM_011510482.1:c.8162A>G (SPEG) XP_011508784.1:p.Gln2721Arg
XM_011510483.1:c.8084A>G (SPEG) XP_011508785.1:p.Gln2695Arg
XM_011510484.1:c.8000A>G (SPEG) XP_011508786.1:p.Gln2667Arg
XR_923921.1:n.353-6810T>C (ASIC4-AS1)
XM_005246242.4:c.5954A>G (SPEG) XP_005246299.1:p.Gln1985Arg
XM_006712189.3:c.8003A>G (SPEG) XP_006712252.1:p.Gln2668Arg
XM_006712193.3:c.5768A>G (SPEG) XP_006712256.1:p.Gln1923Arg
XM_011510479.2:c.8345A>G (SPEG) XP_011508781.1:p.Gln2782Arg
XM_011510483.2:c.8063A>G (SPEG) XP_011508785.2:p.Gln2688Arg
XM_017003157.1:c.8063A>G (SPEG) XP_016858646.1:p.Gln2688Arg
XM_017003158.2:c.5768A>G (SPEG) XP_016858647.1:p.Gln1923Arg
XM_017003160.1:c.3323A>G (SPEG) XP_016858649.1:p.Gln1108Arg
XR_923921.2:n.392-6810T>C (ASIC4-AS1)
NM_005876.5:c.8315A>G (SPEG) MANE Select NP_005867.3:p.Gln2772Arg