Canonical Allele Identifier: CA350708846
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489210G>C , CM000664.2:g.219489210G>C GRCh38
NC_000002.11:g.220353932G>C , CM000664.1:g.220353932G>C GRCh37
NC_000002.10:g.220062176G>C NCBI36
NG_051022.1:g.59996G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8306G>C (SPEG) MANE Select ENSP00000311684.7:p.Arg2769Thr
ENST00000312358.11:c.8306G>C (SPEG) ENSP00000311684.7:p.Arg2769Thr
ENST00000485813.5:n.7549G>C (SPEG)
NM_005876.4:c.8306G>C (SPEG) NP_005867.3:p.Arg2769Thr
XM_005246237.2:c.8024G>C (SPEG) XP_005246294.1:p.Arg2675Thr
XM_005246239.2:c.5930G>C (SPEG) XP_005246296.1:p.Arg1977Thr
XM_005246240.2:c.5759G>C (SPEG) XP_005246297.1:p.Arg1920Thr
XM_005246241.1:c.5759G>C (SPEG) XP_005246298.1:p.Arg1920Thr
XM_005246242.3:c.5945G>C (SPEG) XP_005246299.1:p.Arg1982Thr
XM_006712189.2:c.7994G>C (SPEG) XP_006712252.1:p.Arg2665Thr
XM_006712193.2:c.5759G>C (SPEG) XP_006712256.1:p.Arg1920Thr
XM_011510479.1:c.8336G>C (SPEG) XP_011508781.1:p.Arg2779Thr
XM_011510480.1:c.8168G>C (SPEG) XP_011508782.1:p.Arg2723Thr
XM_011510481.1:c.8159G>C (SPEG) XP_011508783.1:p.Arg2720Thr
XM_011510482.1:c.8153G>C (SPEG) XP_011508784.1:p.Arg2718Thr
XM_011510483.1:c.8075G>C (SPEG) XP_011508785.1:p.Arg2692Thr
XM_011510484.1:c.7991G>C (SPEG) XP_011508786.1:p.Arg2664Thr
XR_923921.1:n.353-6801C>G (ASIC4-AS1)
XM_005246242.4:c.5945G>C (SPEG) XP_005246299.1:p.Arg1982Thr
XM_006712189.3:c.7994G>C (SPEG) XP_006712252.1:p.Arg2665Thr
XM_006712193.3:c.5759G>C (SPEG) XP_006712256.1:p.Arg1920Thr
XM_011510479.2:c.8336G>C (SPEG) XP_011508781.1:p.Arg2779Thr
XM_011510483.2:c.8054G>C (SPEG) XP_011508785.2:p.Arg2685Thr
XM_017003157.1:c.8054G>C (SPEG) XP_016858646.1:p.Arg2685Thr
XM_017003158.2:c.5759G>C (SPEG) XP_016858647.1:p.Arg1920Thr
XM_017003160.1:c.3314G>C (SPEG) XP_016858649.1:p.Arg1105Thr
XR_923921.2:n.392-6801C>G (ASIC4-AS1)
NM_005876.5:c.8306G>C (SPEG) MANE Select NP_005867.3:p.Arg2769Thr