Canonical Allele Identifier: CA1329242234

Gene: SPEG ASIC4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219489175G= , CM000664.2:g.219489175G=	GRCh38
NC_000002.11:g.220353897G= , CM000664.1:g.220353897G=	GRCh37
NC_000002.10:g.220062141G=	NCBI36
NG_051022.1:g.59961G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.8271G= (SPEG) MANE Select	ENSP00000311684.7:p.Gly2757=
ENST00000312358.11:c.8271G= (SPEG)	ENSP00000311684.7:p.Gly2757=
ENST00000485813.5:n.7514G= (SPEG)
NM_005876.4:c.8271G= (SPEG)	NP_005867.3:p.Gly2757=
XM_005246237.2:c.7989G= (SPEG)	XP_005246294.1:p.Gly2663=
XM_005246239.2:c.5895G= (SPEG)	XP_005246296.1:p.Gly1965=
XM_005246240.2:c.5724G= (SPEG)	XP_005246297.1:p.Gly1908=
XM_005246241.1:c.5724G= (SPEG)	XP_005246298.1:p.Gly1908=
XM_005246242.3:c.5910G= (SPEG)	XP_005246299.1:p.Gly1970=
XM_006712189.2:c.7959G= (SPEG)	XP_006712252.1:p.Gly2653=
XM_006712193.2:c.5724G= (SPEG)	XP_006712256.1:p.Gly1908=
XM_011510479.1:c.8301G= (SPEG)	XP_011508781.1:p.Gly2767=
XM_011510480.1:c.8133G= (SPEG)	XP_011508782.1:p.Gly2711=
XM_011510481.1:c.8124G= (SPEG)	XP_011508783.1:p.Gly2708=
XM_011510482.1:c.8118G= (SPEG)	XP_011508784.1:p.Gly2706=
XM_011510483.1:c.8040G= (SPEG)	XP_011508785.1:p.Gly2680=
XM_011510484.1:c.7956G= (SPEG)	XP_011508786.1:p.Gly2652=
XR_923921.1:n.353-6766C= (ASIC4-AS1)
XM_005246242.4:c.5910G= (SPEG)	XP_005246299.1:p.Gly1970=
XM_006712189.3:c.7959G= (SPEG)	XP_006712252.1:p.Gly2653=
XM_006712193.3:c.5724G= (SPEG)	XP_006712256.1:p.Gly1908=
XM_011510479.2:c.8301G= (SPEG)	XP_011508781.1:p.Gly2767=
XM_011510483.2:c.8019G= (SPEG)	XP_011508785.2:p.Gly2673=
XM_017003157.1:c.8019G= (SPEG)	XP_016858646.1:p.Gly2673=
XM_017003158.2:c.5724G= (SPEG)	XP_016858647.1:p.Gly1908=
XM_017003160.1:c.3279G= (SPEG)	XP_016858649.1:p.Gly1093=
XR_923921.2:n.392-6766C= (ASIC4-AS1)
NM_005876.5:c.8271G= (SPEG) MANE Select	NP_005867.3:p.Gly2757=