Canonical Allele Identifier: CA1329242198

Gene: SPEG ASIC4-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219489102A= , CM000664.2:g.219489102A=	GRCh38
NC_000002.11:g.220353824A= , CM000664.1:g.220353824A=	GRCh37
NC_000002.10:g.220062068A=	NCBI36
NG_051022.1:g.59888A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312358.12:c.8198A= (SPEG) MANE Select	ENSP00000311684.7:p.Tyr2733=
ENST00000312358.11:c.8198A= (SPEG)	ENSP00000311684.7:p.Tyr2733=
ENST00000485813.5:n.7441A= (SPEG)
NM_005876.4:c.8198A= (SPEG)	NP_005867.3:p.Tyr2733=
XM_005246237.2:c.7916A= (SPEG)	XP_005246294.1:p.Tyr2639=
XM_005246239.2:c.5822A= (SPEG)	XP_005246296.1:p.Tyr1941=
XM_005246240.2:c.5651A= (SPEG)	XP_005246297.1:p.Tyr1884=
XM_005246241.1:c.5651A= (SPEG)	XP_005246298.1:p.Tyr1884=
XM_005246242.3:c.5837A= (SPEG)	XP_005246299.1:p.Tyr1946=
XM_006712189.2:c.7886A= (SPEG)	XP_006712252.1:p.Tyr2629=
XM_006712193.2:c.5651A= (SPEG)	XP_006712256.1:p.Tyr1884=
XM_011510479.1:c.8228A= (SPEG)	XP_011508781.1:p.Tyr2743=
XM_011510480.1:c.8060A= (SPEG)	XP_011508782.1:p.Tyr2687=
XM_011510481.1:c.8051A= (SPEG)	XP_011508783.1:p.Tyr2684=
XM_011510482.1:c.8045A= (SPEG)	XP_011508784.1:p.Tyr2682=
XM_011510483.1:c.7967A= (SPEG)	XP_011508785.1:p.Tyr2656=
XM_011510484.1:c.7883A= (SPEG)	XP_011508786.1:p.Tyr2628=
XR_923921.1:n.353-6693T= (ASIC4-AS1)
XM_005246242.4:c.5837A= (SPEG)	XP_005246299.1:p.Tyr1946=
XM_006712189.3:c.7886A= (SPEG)	XP_006712252.1:p.Tyr2629=
XM_006712193.3:c.5651A= (SPEG)	XP_006712256.1:p.Tyr1884=
XM_011510479.2:c.8228A= (SPEG)	XP_011508781.1:p.Tyr2743=
XM_011510483.2:c.7946A= (SPEG)	XP_011508785.2:p.Tyr2649=
XM_017003157.1:c.7946A= (SPEG)	XP_016858646.1:p.Tyr2649=
XM_017003158.2:c.5651A= (SPEG)	XP_016858647.1:p.Tyr1884=
XM_017003160.1:c.3206A= (SPEG)	XP_016858649.1:p.Tyr1069=
XR_923921.2:n.392-6693T= (ASIC4-AS1)
NM_005876.5:c.8198A= (SPEG) MANE Select	NP_005867.3:p.Tyr2733=