Canonical Allele Identifier: CA350708695
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489140T>C , CM000664.2:g.219489140T>C GRCh38
NC_000002.11:g.220353862T>C , CM000664.1:g.220353862T>C GRCh37
NC_000002.10:g.220062106T>C NCBI36
NG_051022.1:g.59926T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8236T>C (SPEG) MANE Select ENSP00000311684.7:p.Phe2746Leu
ENST00000312358.11:c.8236T>C (SPEG) ENSP00000311684.7:p.Phe2746Leu
ENST00000485813.5:n.7479T>C (SPEG)
NM_005876.4:c.8236T>C (SPEG) NP_005867.3:p.Phe2746Leu
XM_005246237.2:c.7954T>C (SPEG) XP_005246294.1:p.Phe2652Leu
XM_005246239.2:c.5860T>C (SPEG) XP_005246296.1:p.Phe1954Leu
XM_005246240.2:c.5689T>C (SPEG) XP_005246297.1:p.Phe1897Leu
XM_005246241.1:c.5689T>C (SPEG) XP_005246298.1:p.Phe1897Leu
XM_005246242.3:c.5875T>C (SPEG) XP_005246299.1:p.Phe1959Leu
XM_006712189.2:c.7924T>C (SPEG) XP_006712252.1:p.Phe2642Leu
XM_006712193.2:c.5689T>C (SPEG) XP_006712256.1:p.Phe1897Leu
XM_011510479.1:c.8266T>C (SPEG) XP_011508781.1:p.Phe2756Leu
XM_011510480.1:c.8098T>C (SPEG) XP_011508782.1:p.Phe2700Leu
XM_011510481.1:c.8089T>C (SPEG) XP_011508783.1:p.Phe2697Leu
XM_011510482.1:c.8083T>C (SPEG) XP_011508784.1:p.Phe2695Leu
XM_011510483.1:c.8005T>C (SPEG) XP_011508785.1:p.Phe2669Leu
XM_011510484.1:c.7921T>C (SPEG) XP_011508786.1:p.Phe2641Leu
XR_923921.1:n.353-6731A>G (ASIC4-AS1)
XM_005246242.4:c.5875T>C (SPEG) XP_005246299.1:p.Phe1959Leu
XM_006712189.3:c.7924T>C (SPEG) XP_006712252.1:p.Phe2642Leu
XM_006712193.3:c.5689T>C (SPEG) XP_006712256.1:p.Phe1897Leu
XM_011510479.2:c.8266T>C (SPEG) XP_011508781.1:p.Phe2756Leu
XM_011510483.2:c.7984T>C (SPEG) XP_011508785.2:p.Phe2662Leu
XM_017003157.1:c.7984T>C (SPEG) XP_016858646.1:p.Phe2662Leu
XM_017003158.2:c.5689T>C (SPEG) XP_016858647.1:p.Phe1897Leu
XM_017003160.1:c.3244T>C (SPEG) XP_016858649.1:p.Phe1082Leu
XR_923921.2:n.392-6731A>G (ASIC4-AS1)
NM_005876.5:c.8236T>C (SPEG) MANE Select NP_005867.3:p.Phe2746Leu