Canonical Allele Identifier: CA2663271190
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489257G>A , CM000664.2:g.219489257G>A GRCh38
NC_000002.11:g.220353979G>A , CM000664.1:g.220353979G>A GRCh37
NC_000002.10:g.220062223G>A NCBI36
NG_051022.1:g.60043G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8317+36G>A (SPEG) MANE Select ENSP00000311684.7:n.8317+36G>A
ENST00000312358.11:c.8317+36G>A (SPEG) ENSP00000311684.7:n.8317+36G>A
ENST00000485813.5:n.7560+36G>A (SPEG)
NM_005876.4:c.8317+36G>A (SPEG) NP_005867.3:n.8317+36G>A
XM_005246237.2:c.8035+36G>A (SPEG) XP_005246294.1:n.8035+36G>A
XM_005246239.2:c.5941+36G>A (SPEG) XP_005246296.1:n.5941+36G>A
XM_005246240.2:c.5770+36G>A (SPEG) XP_005246297.1:n.5770+36G>A
XM_005246241.1:c.5770+36G>A (SPEG) XP_005246298.1:n.5770+36G>A
XM_005246242.3:c.5956+36G>A (SPEG) XP_005246299.1:n.5956+36G>A
XM_006712189.2:c.8005+36G>A (SPEG) XP_006712252.1:n.8005+36G>A
XM_006712193.2:c.5770+36G>A (SPEG) XP_006712256.1:n.5770+36G>A
XM_011510479.1:c.8347+36G>A (SPEG) XP_011508781.1:n.8347+36G>A
XM_011510480.1:c.8179+36G>A (SPEG) XP_011508782.1:n.8179+36G>A
XM_011510481.1:c.8170+36G>A (SPEG) XP_011508783.1:n.8170+36G>A
XM_011510482.1:c.8164+36G>A (SPEG) XP_011508784.1:n.8164+36G>A
XM_011510483.1:c.8086+36G>A (SPEG) XP_011508785.1:n.8086+36G>A
XM_011510484.1:c.8002+36G>A (SPEG) XP_011508786.1:n.8002+36G>A
XR_923921.1:n.353-6848C>T (ASIC4-AS1)
XM_005246242.4:c.5956+36G>A (SPEG) XP_005246299.1:n.5956+36G>A
XM_006712189.3:c.8005+36G>A (SPEG) XP_006712252.1:n.8005+36G>A
XM_006712193.3:c.5770+36G>A (SPEG) XP_006712256.1:n.5770+36G>A
XM_011510479.2:c.8347+36G>A (SPEG) XP_011508781.1:n.8347+36G>A
XM_011510483.2:c.8065+36G>A (SPEG) XP_011508785.2:n.8065+36G>A
XM_017003157.1:c.8065+36G>A (SPEG) XP_016858646.1:n.8065+36G>A
XM_017003158.2:c.5770+36G>A (SPEG) XP_016858647.1:n.5770+36G>A
XM_017003160.1:c.3325+36G>A (SPEG) XP_016858649.1:n.3325+36G>A
XR_923921.2:n.392-6848C>T (ASIC4-AS1)
NM_005876.5:c.8317+36G>A (SPEG) MANE Select NP_005867.3:n.8317+36G>A