Canonical Allele Identifier: CA431431476

Gene: SPEG ASIC4-AS1

Linked Data

• MyVariant Identifiers: chr2:g.220353918G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219489196G>A , CM000664.2:g.219489196G>A	GRCh38
NC_000002.11:g.220353918G>A , CM000664.1:g.220353918G>A	GRCh37
NC_000002.10:g.220062162G>A	NCBI36
NG_051022.1:g.59982G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.8292G>A (SPEG) MANE Select	ENSP00000311684.7:p.Glu2764=
ENST00000312358.11:c.8292G>A (SPEG)	ENSP00000311684.7:p.Glu2764=
ENST00000485813.5:n.7535G>A (SPEG)
NM_005876.4:c.8292G>A (SPEG)	NP_005867.3:p.Glu2764=
XM_005246237.2:c.8010G>A (SPEG)	XP_005246294.1:p.Glu2670=
XM_005246239.2:c.5916G>A (SPEG)	XP_005246296.1:p.Glu1972=
XM_005246240.2:c.5745G>A (SPEG)	XP_005246297.1:p.Glu1915=
XM_005246241.1:c.5745G>A (SPEG)	XP_005246298.1:p.Glu1915=
XM_005246242.3:c.5931G>A (SPEG)	XP_005246299.1:p.Glu1977=
XM_006712189.2:c.7980G>A (SPEG)	XP_006712252.1:p.Glu2660=
XM_006712193.2:c.5745G>A (SPEG)	XP_006712256.1:p.Glu1915=
XM_011510479.1:c.8322G>A (SPEG)	XP_011508781.1:p.Glu2774=
XM_011510480.1:c.8154G>A (SPEG)	XP_011508782.1:p.Glu2718=
XM_011510481.1:c.8145G>A (SPEG)	XP_011508783.1:p.Glu2715=
XM_011510482.1:c.8139G>A (SPEG)	XP_011508784.1:p.Glu2713=
XM_011510483.1:c.8061G>A (SPEG)	XP_011508785.1:p.Glu2687=
XM_011510484.1:c.7977G>A (SPEG)	XP_011508786.1:p.Glu2659=
XR_923921.1:n.353-6787C>T (ASIC4-AS1)
XM_005246242.4:c.5931G>A (SPEG)	XP_005246299.1:p.Glu1977=
XM_006712189.3:c.7980G>A (SPEG)	XP_006712252.1:p.Glu2660=
XM_006712193.3:c.5745G>A (SPEG)	XP_006712256.1:p.Glu1915=
XM_011510479.2:c.8322G>A (SPEG)	XP_011508781.1:p.Glu2774=
XM_011510483.2:c.8040G>A (SPEG)	XP_011508785.2:p.Glu2680=
XM_017003157.1:c.8040G>A (SPEG)	XP_016858646.1:p.Glu2680=
XM_017003158.2:c.5745G>A (SPEG)	XP_016858647.1:p.Glu1915=
XM_017003160.1:c.3300G>A (SPEG)	XP_016858649.1:p.Glu1100=
XR_923921.2:n.392-6787C>T (ASIC4-AS1)
NM_005876.5:c.8292G>A (SPEG) MANE Select	NP_005867.3:p.Glu2764=