Canonical Allele Identifier: CA2819314655

Gene: SCO2 NCAPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523569T>A , CM000684.2:g.50523569T>A	GRCh38
NC_000022.10:g.50961998T>A , CM000684.1:g.50961998T>A	GRCh37
NC_000022.9:g.49308864T>A	NCBI36
NG_016235.1:g.7871A>T
NG_021419.1:g.20354T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395693.8:c.*42A>T (SCO2) MANE Select	ENSP00000379046.4:n.*42A>T
ENST00000420993.7:c.*194T>A (NCAPH2) MANE Select	ENSP00000410088.2:n.*194T>A
ENST00000395693.7:c.*42A>T	ENSP00000379046.3:n.*42A>T
ENST00000535425.5:c.*42A>T	ENSP00000444242.1:n.*42A>T
ENST00000543927.5:c.*42A>T	ENSP00000444433.1:n.*42A>T
NM_001169109.1:c.*42A>T (SCO2)	NP_001162580.1:n.*42A>T
NM_001169110.1:c.*42A>T (SCO2)	NP_001162581.1:n.*42A>T
NM_001169111.1:c.*42A>T (SCO2)	NP_001162582.1:n.*42A>T
NM_001185011.1:c.*194T>A (NCAPH2)	NP_001171940.1:n.*194T>A
NM_005138.2:c.*42A>T (SCO2)	NP_005129.2:n.*42A>T
NM_152299.3:c.*194T>A (NCAPH2)	NP_689512.2:n.*194T>A
XR_001755232.1:n.2222T>A (NCAPH2)
NM_152299.4:c.*194T>A (NCAPH2) MANE Select	NP_689512.2:n.*194T>A
NM_001185011.2:c.*194T>A (NCAPH2)	NP_001171940.1:n.*194T>A
NM_005138.3:c.*42A>T (SCO2) MANE Select	NP_005129.2:n.*42A>T
NM_001169109.2:c.*42A>T (SCO2)	NP_001162580.1:n.*42A>T
NM_001169111.2:c.*42A>T (SCO2)	NP_001162582.1:n.*42A>T