Canonical Allele Identifier: CA1329242232

Gene: SPEG ASIC4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219489169G= , CM000664.2:g.219489169G=	GRCh38
NC_000002.11:g.220353891G= , CM000664.1:g.220353891G=	GRCh37
NC_000002.10:g.220062135G=	NCBI36
NG_051022.1:g.59955G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.8265G= (SPEG) MANE Select	ENSP00000311684.7:p.Gly2755=
ENST00000312358.11:c.8265G= (SPEG)	ENSP00000311684.7:p.Gly2755=
ENST00000485813.5:n.7508G= (SPEG)
NM_005876.4:c.8265G= (SPEG)	NP_005867.3:p.Gly2755=
XM_005246237.2:c.7983G= (SPEG)	XP_005246294.1:p.Gly2661=
XM_005246239.2:c.5889G= (SPEG)	XP_005246296.1:p.Gly1963=
XM_005246240.2:c.5718G= (SPEG)	XP_005246297.1:p.Gly1906=
XM_005246241.1:c.5718G= (SPEG)	XP_005246298.1:p.Gly1906=
XM_005246242.3:c.5904G= (SPEG)	XP_005246299.1:p.Gly1968=
XM_006712189.2:c.7953G= (SPEG)	XP_006712252.1:p.Gly2651=
XM_006712193.2:c.5718G= (SPEG)	XP_006712256.1:p.Gly1906=
XM_011510479.1:c.8295G= (SPEG)	XP_011508781.1:p.Gly2765=
XM_011510480.1:c.8127G= (SPEG)	XP_011508782.1:p.Gly2709=
XM_011510481.1:c.8118G= (SPEG)	XP_011508783.1:p.Gly2706=
XM_011510482.1:c.8112G= (SPEG)	XP_011508784.1:p.Gly2704=
XM_011510483.1:c.8034G= (SPEG)	XP_011508785.1:p.Gly2678=
XM_011510484.1:c.7950G= (SPEG)	XP_011508786.1:p.Gly2650=
XR_923921.1:n.353-6760C= (ASIC4-AS1)
XM_005246242.4:c.5904G= (SPEG)	XP_005246299.1:p.Gly1968=
XM_006712189.3:c.7953G= (SPEG)	XP_006712252.1:p.Gly2651=
XM_006712193.3:c.5718G= (SPEG)	XP_006712256.1:p.Gly1906=
XM_011510479.2:c.8295G= (SPEG)	XP_011508781.1:p.Gly2765=
XM_011510483.2:c.8013G= (SPEG)	XP_011508785.2:p.Gly2671=
XM_017003157.1:c.8013G= (SPEG)	XP_016858646.1:p.Gly2671=
XM_017003158.2:c.5718G= (SPEG)	XP_016858647.1:p.Gly1906=
XM_017003160.1:c.3273G= (SPEG)	XP_016858649.1:p.Gly1091=
XR_923921.2:n.392-6760C= (ASIC4-AS1)
NM_005876.5:c.8265G= (SPEG) MANE Select	NP_005867.3:p.Gly2755=