Canonical Allele Identifier: CA1329242240

Gene: SPEG ASIC4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219489200G= , CM000664.2:g.219489200G=	GRCh38
NC_000002.11:g.220353922G= , CM000664.1:g.220353922G=	GRCh37
NC_000002.10:g.220062166G=	NCBI36
NG_051022.1:g.59986G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.8296G= (SPEG) MANE Select	ENSP00000311684.7:p.Val2766=
ENST00000312358.11:c.8296G= (SPEG)	ENSP00000311684.7:p.Val2766=
ENST00000485813.5:n.7539G= (SPEG)
NM_005876.4:c.8296G= (SPEG)	NP_005867.3:p.Val2766=
XM_005246237.2:c.8014G= (SPEG)	XP_005246294.1:p.Val2672=
XM_005246239.2:c.5920G= (SPEG)	XP_005246296.1:p.Val1974=
XM_005246240.2:c.5749G= (SPEG)	XP_005246297.1:p.Val1917=
XM_005246241.1:c.5749G= (SPEG)	XP_005246298.1:p.Val1917=
XM_005246242.3:c.5935G= (SPEG)	XP_005246299.1:p.Val1979=
XM_006712189.2:c.7984G= (SPEG)	XP_006712252.1:p.Val2662=
XM_006712193.2:c.5749G= (SPEG)	XP_006712256.1:p.Val1917=
XM_011510479.1:c.8326G= (SPEG)	XP_011508781.1:p.Val2776=
XM_011510480.1:c.8158G= (SPEG)	XP_011508782.1:p.Val2720=
XM_011510481.1:c.8149G= (SPEG)	XP_011508783.1:p.Val2717=
XM_011510482.1:c.8143G= (SPEG)	XP_011508784.1:p.Val2715=
XM_011510483.1:c.8065G= (SPEG)	XP_011508785.1:p.Val2689=
XM_011510484.1:c.7981G= (SPEG)	XP_011508786.1:p.Val2661=
XR_923921.1:n.353-6791C= (ASIC4-AS1)
XM_005246242.4:c.5935G= (SPEG)	XP_005246299.1:p.Val1979=
XM_006712189.3:c.7984G= (SPEG)	XP_006712252.1:p.Val2662=
XM_006712193.3:c.5749G= (SPEG)	XP_006712256.1:p.Val1917=
XM_011510479.2:c.8326G= (SPEG)	XP_011508781.1:p.Val2776=
XM_011510483.2:c.8044G= (SPEG)	XP_011508785.2:p.Val2682=
XM_017003157.1:c.8044G= (SPEG)	XP_016858646.1:p.Val2682=
XM_017003158.2:c.5749G= (SPEG)	XP_016858647.1:p.Val1917=
XM_017003160.1:c.3304G= (SPEG)	XP_016858649.1:p.Val1102=
XR_923921.2:n.392-6791C= (ASIC4-AS1)
NM_005876.5:c.8296G= (SPEG) MANE Select	NP_005867.3:p.Val2766=