Canonical Allele Identifier: CA2657556765

Gene: SCO2 NCAPH2

Linked Data

• gnomAD v4: 22-50523980-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523981dup , CM000684.2:g.50523981dup	GRCh38
NC_000022.10:g.50962410dup , CM000684.1:g.50962410dup	GRCh37
NC_000022.9:g.49309276dup	NCBI36
NG_011860.1:g.11105dup , LRG_727:g.11105dup
NG_016235.1:g.7459dup
NG_021419.1:g.20766dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395693.8:c.431dup (SCO2) MANE Select	ENSP00000379046.4:p.Val145GlyfsTer?
ENST00000420993.7:c.*606dup (NCAPH2) MANE Select	ENSP00000410088.2:n.*606dup
ENST00000543927.6:c.431dup (SCO2)	ENSP00000444433.1:p.Val145GlyfsTer?
ENST00000638598.2:c.431dup (SCO2)	ENSP00000491753.2:p.Val145GlyfsTer?
ENST00000252785.3:c.431dup	ENSP00000252785.3:p.Val145GlyfsTer?
ENST00000395693.7:c.431dup	ENSP00000379046.3:p.Val145GlyfsTer?
ENST00000535425.5:c.431dup	ENSP00000444242.1:p.Val145GlyfsTer?
ENST00000543927.5:c.431dup	ENSP00000444433.1:p.Val145GlyfsTer?
NM_001169109.1:c.431dup (SCO2)	NP_001162580.1:p.Val145GlyfsTer?
NM_001169110.1:c.431dup (SCO2)	NP_001162581.1:p.Val145GlyfsTer?
NM_001169111.1:c.431dup (SCO2)	NP_001162582.1:p.Val145GlyfsTer?
NM_001185011.1:c.*606dup (NCAPH2)	NP_001171940.1:n.*606dup
NM_005138.2:c.431dup (SCO2)	NP_005129.2:p.Val145GlyfsTer?
NM_152299.3:c.*606dup (NCAPH2)	NP_689512.2:n.*606dup
XR_001755232.1:n.2634dup (NCAPH2)
NM_152299.4:c.*606dup (NCAPH2) MANE Select	NP_689512.2:n.*606dup
NM_001185011.2:c.*606dup (NCAPH2)	NP_001171940.1:n.*606dup
NM_005138.3:c.431dup (SCO2) MANE Select	NP_005129.2:p.Val145GlyfsTer?
NM_001169109.2:c.431dup (SCO2)	NP_001162580.1:p.Val145GlyfsTer?
NM_001169111.2:c.431dup (SCO2)	NP_001162582.1:p.Val145GlyfsTer?