Canonical Allele Identifier: CA754071390

Linked Data

dbSNP Id: rs1170373128

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50524361_50524380dup , CM000684.2:g.50524361_50524380dup GRCh38
NC_000022.10:g.50962790_50962809dup , CM000684.1:g.50962790_50962809dup GRCh37
NC_000022.9:g.49309656_49309675dup NCBI36
NG_011860.1:g.10706_10725dup , LRG_727:g.10706_10725dup
NG_016235.1:g.7060_7079dup
NG_021419.1:g.21146_21165dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395693.8:c.32_51dup (SCO2) MANE Select ENSP00000379046.4:p.Lys18GlyfsTer23
ENST00000420993.7:c.*986_*1005dup (NCAPH2) MANE Select ENSP00000410088.2:n.*986_*1005dup
ENST00000543927.6:c.32_51dup (SCO2) ENSP00000444433.1:p.Lys18GlyfsTer23
ENST00000638598.2:c.32_51dup (SCO2) ENSP00000491753.2:p.Lys18GlyfsTer23
ENST00000252785.3:c.32_51dup ENSP00000252785.3:p.Lys18GlyfsTer23
ENST00000395693.7:c.32_51dup ENSP00000379046.3:p.Lys18GlyfsTer23
ENST00000423348.1:c.32_51dup ENSP00000403570.1:p.Lys18GlyfsTer23
ENST00000439934.5:c.32_51dup ENSP00000415642.1:p.Lys18GlyfsTer23
ENST00000535425.5:c.32_51dup ENSP00000444242.1:p.Lys18GlyfsTer23
ENST00000543927.5:c.32_51dup ENSP00000444433.1:p.Lys18GlyfsTer23
NM_001169109.1:c.32_51dup (SCO2) NP_001162580.1:p.Lys18GlyfsTer23
NM_001169110.1:c.32_51dup (SCO2) NP_001162581.1:p.Lys18GlyfsTer23
NM_001169111.1:c.32_51dup (SCO2) NP_001162582.1:p.Lys18GlyfsTer23
NM_001185011.1:c.*986_*1005dup (NCAPH2) NP_001171940.1:n.*986_*1005dup
NM_005138.2:c.32_51dup (SCO2) NP_005129.2:p.Lys18GlyfsTer23
NM_152299.3:c.*986_*1005dup (NCAPH2) NP_689512.2:n.*986_*1005dup
XR_001755232.1:n.3014_3033dup (NCAPH2)
NM_152299.4:c.*986_*1005dup (NCAPH2) MANE Select NP_689512.2:n.*986_*1005dup
NM_001185011.2:c.*986_*1005dup (NCAPH2) NP_001171940.1:n.*986_*1005dup
NM_005138.3:c.32_51dup (SCO2) MANE Select NP_005129.2:p.Lys18GlyfsTer23
NM_001169109.2:c.32_51dup (SCO2) NP_001162580.1:p.Lys18GlyfsTer23
NM_001169111.2:c.32_51dup (SCO2) NP_001162582.1:p.Lys18GlyfsTer23