Canonical Allele Identifier: CA10321202

Gene: SCO2 NCAPH2

Linked Data

• ClinVar Variation Id: 706220
• ClinVar RCV Id: RCV000876757
• dbSNP Id: rs536037216
• ExAC: 22:50962385 T / A
• gnomAD v2: 22-50962385-T-A
• gnomAD v3: 22-50523956-T-A
• gnomAD v4: 22-50523956-T-A
• MyVariant Identifiers: chr22:g.50962385T>A (hg19) ; chr22:g.50523956T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523956T>A , CM000684.2:g.50523956T>A	GRCh38
NC_000022.10:g.50962385T>A , CM000684.1:g.50962385T>A	GRCh37
NC_000022.9:g.49309251T>A	NCBI36
NG_011860.1:g.11130A>T , LRG_727:g.11130A>T
NG_016235.1:g.7484A>T
NG_021419.1:g.20741T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395693.8:c.456A>T (SCO2) MANE Select	ENSP00000379046.4:p.Glu152Asp
ENST00000420993.7:c.*581T>A (NCAPH2) MANE Select	ENSP00000410088.2:n.*581T>A
ENST00000543927.6:c.456A>T (SCO2)	ENSP00000444433.1:p.Glu152Asp
ENST00000638598.2:c.456A>T (SCO2)	ENSP00000491753.2:p.Glu152Asp
ENST00000252785.3:c.456A>T	ENSP00000252785.3:p.Glu152Asp
ENST00000395693.7:c.456A>T	ENSP00000379046.3:p.Glu152Asp
ENST00000535425.5:c.456A>T	ENSP00000444242.1:p.Glu152Asp
ENST00000543927.5:c.456A>T	ENSP00000444433.1:p.Glu152Asp
NM_001169109.1:c.456A>T (SCO2)	NP_001162580.1:p.Glu152Asp
NM_001169110.1:c.456A>T (SCO2)	NP_001162581.1:p.Glu152Asp
NM_001169111.1:c.456A>T (SCO2)	NP_001162582.1:p.Glu152Asp
NM_001185011.1:c.*581T>A (NCAPH2)	NP_001171940.1:n.*581T>A
NM_005138.2:c.456A>T (SCO2)	NP_005129.2:p.Glu152Asp
NM_152299.3:c.*581T>A (NCAPH2)	NP_689512.2:n.*581T>A
XR_001755232.1:n.2609T>A (NCAPH2)
NM_152299.4:c.*581T>A (NCAPH2) MANE Select	NP_689512.2:n.*581T>A
NM_001185011.2:c.*581T>A (NCAPH2)	NP_001171940.1:n.*581T>A
NM_005138.3:c.456A>T (SCO2) MANE Select	NP_005129.2:p.Glu152Asp
NM_001169109.2:c.456A>T (SCO2)	NP_001162580.1:p.Glu152Asp
NM_001169111.2:c.456A>T (SCO2)	NP_001162582.1:p.Glu152Asp