Canonical Allele Identifier: CA2410905804

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50523624C= , CM000684.2:g.50523624C= GRCh38
NC_000022.10:g.50962053C= , CM000684.1:g.50962053C= GRCh37
NC_000022.9:g.49308919C= NCBI36
NG_016235.1:g.7816G=
NG_021419.1:g.20409C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395693.8:c.788G= (SCO2) MANE Select ENSP00000379046.4:p.Ser263=
ENST00000420993.7:c.*249C= (NCAPH2) MANE Select ENSP00000410088.2:n.*249C=
ENST00000543927.6:c.788G= (SCO2) ENSP00000444433.1:p.Ser263=
ENST00000252785.3:c.788G= ENSP00000252785.3:p.Ser263=
ENST00000395693.7:c.788G= ENSP00000379046.3:p.Ser263=
ENST00000535425.5:c.788G= ENSP00000444242.1:p.Ser263=
ENST00000543927.5:c.788G= ENSP00000444433.1:p.Ser263=
NM_001169109.1:c.788G= (SCO2) NP_001162580.1:p.Ser263=
NM_001169110.1:c.788G= (SCO2) NP_001162581.1:p.Ser263=
NM_001169111.1:c.788G= (SCO2) NP_001162582.1:p.Ser263=
NM_001185011.1:c.*249C= (NCAPH2) NP_001171940.1:n.*249C=
NM_005138.2:c.788G= (SCO2) NP_005129.2:p.Ser263=
NM_152299.3:c.*249C= (NCAPH2) NP_689512.2:n.*249C=
XR_001755232.1:n.2277C= (NCAPH2)
NM_152299.4:c.*249C= (NCAPH2) MANE Select NP_689512.2:n.*249C=
NM_001185011.2:c.*249C= (NCAPH2) NP_001171940.1:n.*249C=
NM_005138.3:c.788G= (SCO2) MANE Select NP_005129.2:p.Ser263=
NM_001169109.2:c.788G= (SCO2) NP_001162580.1:p.Ser263=
NM_001169111.2:c.788G= (SCO2) NP_001162582.1:p.Ser263=