Canonical Allele Identifier: CA2410905811

Gene: SCO2 NCAPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523636G= , CM000684.2:g.50523636G=	GRCh38
NC_000022.10:g.50962065G= , CM000684.1:g.50962065G=	GRCh37
NC_000022.9:g.49308931G=	NCBI36
NG_016235.1:g.7804C=
NG_021419.1:g.20421G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395693.8:c.776C= (SCO2) MANE Select	ENSP00000379046.4:p.Ala259=
ENST00000420993.7:c.*261G= (NCAPH2) MANE Select	ENSP00000410088.2:n.*261G=
ENST00000543927.6:c.776C= (SCO2)	ENSP00000444433.1:p.Ala259=
ENST00000252785.3:c.776C=	ENSP00000252785.3:p.Ala259=
ENST00000395693.7:c.776C=	ENSP00000379046.3:p.Ala259=
ENST00000535425.5:c.776C=	ENSP00000444242.1:p.Ala259=
ENST00000543927.5:c.776C=	ENSP00000444433.1:p.Ala259=
NM_001169109.1:c.776C= (SCO2)	NP_001162580.1:p.Ala259=
NM_001169110.1:c.776C= (SCO2)	NP_001162581.1:p.Ala259=
NM_001169111.1:c.776C= (SCO2)	NP_001162582.1:p.Ala259=
NM_001185011.1:c.*261G= (NCAPH2)	NP_001171940.1:n.*261G=
NM_005138.2:c.776C= (SCO2)	NP_005129.2:p.Ala259=
NM_152299.3:c.*261G= (NCAPH2)	NP_689512.2:n.*261G=
XR_001755232.1:n.2289G= (NCAPH2)
NM_152299.4:c.*261G= (NCAPH2) MANE Select	NP_689512.2:n.*261G=
NM_001185011.2:c.*261G= (NCAPH2)	NP_001171940.1:n.*261G=
NM_005138.3:c.776C= (SCO2) MANE Select	NP_005129.2:p.Ala259=
NM_001169109.2:c.776C= (SCO2)	NP_001162580.1:p.Ala259=
NM_001169111.2:c.776C= (SCO2)	NP_001162582.1:p.Ala259=