Canonical Allele Identifier: CA2410905899

Gene: SCO2 NCAPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523785G= , CM000684.2:g.50523785G=	GRCh38
NC_000022.10:g.50962214G= , CM000684.1:g.50962214G=	GRCh37
NC_000022.9:g.49309080G=	NCBI36
NG_011860.1:g.11301C= , LRG_727:g.11301C=
NG_016235.1:g.7655C=
NG_021419.1:g.20570G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395693.8:c.627C= (SCO2) MANE Select	ENSP00000379046.4:p.Tyr209=
ENST00000420993.7:c.*410G= (NCAPH2) MANE Select	ENSP00000410088.2:n.*410G=
ENST00000543927.6:c.627C= (SCO2)	ENSP00000444433.1:p.Tyr209=
ENST00000252785.3:c.627C=	ENSP00000252785.3:p.Tyr209=
ENST00000395693.7:c.627C=	ENSP00000379046.3:p.Tyr209=
ENST00000535425.5:c.627C=	ENSP00000444242.1:p.Tyr209=
ENST00000543927.5:c.627C=	ENSP00000444433.1:p.Tyr209=
NM_001169109.1:c.627C= (SCO2)	NP_001162580.1:p.Tyr209=
NM_001169110.1:c.627C= (SCO2)	NP_001162581.1:p.Tyr209=
NM_001169111.1:c.627C= (SCO2)	NP_001162582.1:p.Tyr209=
NM_001185011.1:c.*410G= (NCAPH2)	NP_001171940.1:n.*410G=
NM_005138.2:c.627C= (SCO2)	NP_005129.2:p.Tyr209=
NM_152299.3:c.*410G= (NCAPH2)	NP_689512.2:n.*410G=
XR_001755232.1:n.2438G= (NCAPH2)
NM_152299.4:c.*410G= (NCAPH2) MANE Select	NP_689512.2:n.*410G=
NM_001185011.2:c.*410G= (NCAPH2)	NP_001171940.1:n.*410G=
NM_005138.3:c.627C= (SCO2) MANE Select	NP_005129.2:p.Tyr209=
NM_001169109.2:c.627C= (SCO2)	NP_001162580.1:p.Tyr209=
NM_001169111.2:c.627C= (SCO2)	NP_001162582.1:p.Tyr209=