Canonical Allele Identifier: CA350708794
Gene: SPEG HGNC NCBI
ASIC4-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219489187C>A , CM000664.2:g.219489187C>A GRCh38
NC_000002.11:g.220353909C>A , CM000664.1:g.220353909C>A GRCh37
NC_000002.10:g.220062153C>A NCBI36
NG_051022.1:g.59973C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312358.12:c.8283C>A (SPEG) MANE Select ENSP00000311684.7:p.Asn2761Lys
ENST00000312358.11:c.8283C>A (SPEG) ENSP00000311684.7:p.Asn2761Lys
ENST00000485813.5:n.7526C>A (SPEG)
NM_005876.4:c.8283C>A (SPEG) NP_005867.3:p.Asn2761Lys
XM_005246237.2:c.8001C>A (SPEG) XP_005246294.1:p.Asn2667Lys
XM_005246239.2:c.5907C>A (SPEG) XP_005246296.1:p.Asn1969Lys
XM_005246240.2:c.5736C>A (SPEG) XP_005246297.1:p.Asn1912Lys
XM_005246241.1:c.5736C>A (SPEG) XP_005246298.1:p.Asn1912Lys
XM_005246242.3:c.5922C>A (SPEG) XP_005246299.1:p.Asn1974Lys
XM_006712189.2:c.7971C>A (SPEG) XP_006712252.1:p.Asn2657Lys
XM_006712193.2:c.5736C>A (SPEG) XP_006712256.1:p.Asn1912Lys
XM_011510479.1:c.8313C>A (SPEG) XP_011508781.1:p.Asn2771Lys
XM_011510480.1:c.8145C>A (SPEG) XP_011508782.1:p.Asn2715Lys
XM_011510481.1:c.8136C>A (SPEG) XP_011508783.1:p.Asn2712Lys
XM_011510482.1:c.8130C>A (SPEG) XP_011508784.1:p.Asn2710Lys
XM_011510483.1:c.8052C>A (SPEG) XP_011508785.1:p.Asn2684Lys
XM_011510484.1:c.7968C>A (SPEG) XP_011508786.1:p.Asn2656Lys
XR_923921.1:n.353-6778G>T (ASIC4-AS1)
XM_005246242.4:c.5922C>A (SPEG) XP_005246299.1:p.Asn1974Lys
XM_006712189.3:c.7971C>A (SPEG) XP_006712252.1:p.Asn2657Lys
XM_006712193.3:c.5736C>A (SPEG) XP_006712256.1:p.Asn1912Lys
XM_011510479.2:c.8313C>A (SPEG) XP_011508781.1:p.Asn2771Lys
XM_011510483.2:c.8031C>A (SPEG) XP_011508785.2:p.Asn2677Lys
XM_017003157.1:c.8031C>A (SPEG) XP_016858646.1:p.Asn2677Lys
XM_017003158.2:c.5736C>A (SPEG) XP_016858647.1:p.Asn1912Lys
XM_017003160.1:c.3291C>A (SPEG) XP_016858649.1:p.Asn1097Lys
XR_923921.2:n.392-6778G>T (ASIC4-AS1)
NM_005876.5:c.8283C>A (SPEG) MANE Select NP_005867.3:p.Asn2761Lys