Canonical Allele Identifier: CA2127709

Gene: SPEG ASIC4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219490807A>G , CM000664.2:g.219490807A>G	GRCh38
NC_000002.11:g.220355529A>G , CM000664.1:g.220355529A>G	GRCh37
NC_000002.10:g.220063773A>G	NCBI36
NG_051022.1:g.61593A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.9236A>G (SPEG) MANE Select	ENSP00000311684.7:p.His3079Arg
ENST00000312358.11:c.9236A>G (SPEG)	ENSP00000311684.7:p.His3079Arg
ENST00000485813.5:n.8479A>G (SPEG)
NM_005876.4:c.9236A>G (SPEG)	NP_005867.3:p.His3079Arg
XM_005246237.2:c.8954A>G (SPEG)	XP_005246294.1:p.His2985Arg
XM_005246239.2:c.6860A>G (SPEG)	XP_005246296.1:p.His2287Arg
XM_005246240.2:c.6689A>G (SPEG)	XP_005246297.1:p.His2230Arg
XM_005246241.1:c.6689A>G (SPEG)	XP_005246298.1:p.His2230Arg
XM_005246242.3:c.6875A>G (SPEG)	XP_005246299.1:p.His2292Arg
XM_006712189.2:c.8924A>G (SPEG)	XP_006712252.1:p.His2975Arg
XM_006712193.2:c.6689A>G (SPEG)	XP_006712256.1:p.His2230Arg
XM_011510479.1:c.9266A>G (SPEG)	XP_011508781.1:p.His3089Arg
XM_011510480.1:c.9098A>G (SPEG)	XP_011508782.1:p.His3033Arg
XM_011510481.1:c.9089A>G (SPEG)	XP_011508783.1:p.His3030Arg
XM_011510482.1:c.9083A>G (SPEG)	XP_011508784.1:p.His3028Arg
XM_011510483.1:c.9005A>G (SPEG)	XP_011508785.1:p.His3002Arg
XM_011510484.1:c.8921A>G (SPEG)	XP_011508786.1:p.His2974Arg
XR_923921.1:n.353-8398T>C (ASIC4-AS1)
XM_005246242.4:c.6875A>G (SPEG)	XP_005246299.1:p.His2292Arg
XM_006712189.3:c.8924A>G (SPEG)	XP_006712252.1:p.His2975Arg
XM_006712193.3:c.6689A>G (SPEG)	XP_006712256.1:p.His2230Arg
XM_011510479.2:c.9266A>G (SPEG)	XP_011508781.1:p.His3089Arg
XM_011510483.2:c.8984A>G (SPEG)	XP_011508785.2:p.His2995Arg
XM_017003157.1:c.8984A>G (SPEG)	XP_016858646.1:p.His2995Arg
XM_017003158.2:c.6689A>G (SPEG)	XP_016858647.1:p.His2230Arg
XM_017003160.1:c.4244A>G (SPEG)	XP_016858649.1:p.His1415Arg
XR_923921.2:n.392-8398T>C (ASIC4-AS1)
NM_005876.5:c.9236A>G (SPEG) MANE Select	NP_005867.3:p.His3079Arg