Canonical Allele Identifier: CA350708868
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489221G>A , CM000664.2:g.219489221G>A GRCh38
NC_000002.11:g.220353943G>A , CM000664.1:g.220353943G>A GRCh37
NC_000002.10:g.220062187G>A NCBI36
NG_051022.1:g.60007G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8317G>A (SPEG) MANE Select ENSP00000311684.7:p.Asp2773Asn
ENST00000312358.11:c.8317G>A (SPEG) ENSP00000311684.7:p.Asp2773Asn
ENST00000485813.5:n.7560G>A (SPEG)
NM_005876.4:c.8317G>A (SPEG) NP_005867.3:p.Asp2773Asn
XM_005246237.2:c.8035G>A (SPEG) XP_005246294.1:p.Asp2679Asn
XM_005246239.2:c.5941G>A (SPEG) XP_005246296.1:p.Asp1981Asn
XM_005246240.2:c.5770G>A (SPEG) XP_005246297.1:p.Asp1924Asn
XM_005246241.1:c.5770G>A (SPEG) XP_005246298.1:p.Asp1924Asn
XM_005246242.3:c.5956G>A (SPEG) XP_005246299.1:p.Asp1986Asn
XM_006712189.2:c.8005G>A (SPEG) XP_006712252.1:p.Asp2669Asn
XM_006712193.2:c.5770G>A (SPEG) XP_006712256.1:p.Asp1924Asn
XM_011510479.1:c.8347G>A (SPEG) XP_011508781.1:p.Asp2783Asn
XM_011510480.1:c.8179G>A (SPEG) XP_011508782.1:p.Asp2727Asn
XM_011510481.1:c.8170G>A (SPEG) XP_011508783.1:p.Asp2724Asn
XM_011510482.1:c.8164G>A (SPEG) XP_011508784.1:p.Asp2722Asn
XM_011510483.1:c.8086G>A (SPEG) XP_011508785.1:p.Asp2696Asn
XM_011510484.1:c.8002G>A (SPEG) XP_011508786.1:p.Asp2668Asn
XR_923921.1:n.353-6812C>T (ASIC4-AS1)
XM_005246242.4:c.5956G>A (SPEG) XP_005246299.1:p.Asp1986Asn
XM_006712189.3:c.8005G>A (SPEG) XP_006712252.1:p.Asp2669Asn
XM_006712193.3:c.5770G>A (SPEG) XP_006712256.1:p.Asp1924Asn
XM_011510479.2:c.8347G>A (SPEG) XP_011508781.1:p.Asp2783Asn
XM_011510483.2:c.8065G>A (SPEG) XP_011508785.2:p.Asp2689Asn
XM_017003157.1:c.8065G>A (SPEG) XP_016858646.1:p.Asp2689Asn
XM_017003158.2:c.5770G>A (SPEG) XP_016858647.1:p.Asp1924Asn
XM_017003160.1:c.3325G>A (SPEG) XP_016858649.1:p.Asp1109Asn
XR_923921.2:n.392-6812C>T (ASIC4-AS1)
NM_005876.5:c.8317G>A (SPEG) MANE Select NP_005867.3:p.Asp2773Asn