Canonical Allele Identifier: CA1329242238

Gene: SPEG ASIC4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219489193T= , CM000664.2:g.219489193T=	GRCh38
NC_000002.11:g.220353915T= , CM000664.1:g.220353915T=	GRCh37
NC_000002.10:g.220062159T=	NCBI36
NG_051022.1:g.59979T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.8289T= (SPEG) MANE Select	ENSP00000311684.7:p.Ser2763=
ENST00000312358.11:c.8289T= (SPEG)	ENSP00000311684.7:p.Ser2763=
ENST00000485813.5:n.7532T= (SPEG)
NM_005876.4:c.8289T= (SPEG)	NP_005867.3:p.Ser2763=
XM_005246237.2:c.8007T= (SPEG)	XP_005246294.1:p.Ser2669=
XM_005246239.2:c.5913T= (SPEG)	XP_005246296.1:p.Ser1971=
XM_005246240.2:c.5742T= (SPEG)	XP_005246297.1:p.Ser1914=
XM_005246241.1:c.5742T= (SPEG)	XP_005246298.1:p.Ser1914=
XM_005246242.3:c.5928T= (SPEG)	XP_005246299.1:p.Ser1976=
XM_006712189.2:c.7977T= (SPEG)	XP_006712252.1:p.Ser2659=
XM_006712193.2:c.5742T= (SPEG)	XP_006712256.1:p.Ser1914=
XM_011510479.1:c.8319T= (SPEG)	XP_011508781.1:p.Ser2773=
XM_011510480.1:c.8151T= (SPEG)	XP_011508782.1:p.Ser2717=
XM_011510481.1:c.8142T= (SPEG)	XP_011508783.1:p.Ser2714=
XM_011510482.1:c.8136T= (SPEG)	XP_011508784.1:p.Ser2712=
XM_011510483.1:c.8058T= (SPEG)	XP_011508785.1:p.Ser2686=
XM_011510484.1:c.7974T= (SPEG)	XP_011508786.1:p.Ser2658=
XR_923921.1:n.353-6784A= (ASIC4-AS1)
XM_005246242.4:c.5928T= (SPEG)	XP_005246299.1:p.Ser1976=
XM_006712189.3:c.7977T= (SPEG)	XP_006712252.1:p.Ser2659=
XM_006712193.3:c.5742T= (SPEG)	XP_006712256.1:p.Ser1914=
XM_011510479.2:c.8319T= (SPEG)	XP_011508781.1:p.Ser2773=
XM_011510483.2:c.8037T= (SPEG)	XP_011508785.2:p.Ser2679=
XM_017003157.1:c.8037T= (SPEG)	XP_016858646.1:p.Ser2679=
XM_017003158.2:c.5742T= (SPEG)	XP_016858647.1:p.Ser1914=
XM_017003160.1:c.3297T= (SPEG)	XP_016858649.1:p.Ser1099=
XR_923921.2:n.392-6784A= (ASIC4-AS1)
NM_005876.5:c.8289T= (SPEG) MANE Select	NP_005867.3:p.Ser2763=