Canonical Allele Identifier: CA1565024346
Gene: SKIC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516560G= , CM000667.2:g.95516560G= GRCh38
NC_000005.9:g.94852264G= , CM000667.1:g.94852264G= GRCh37
NC_000005.8:g.94878020G= NCBI36
NG_023414.1:g.43446C= , LRG_173:g.43446C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000506007.2:n.3082C=
ENST00000513232.2:c.*1507C= ENSP00000422749.2:n.*1507C=
ENST00000698450.1:n.1926C=
ENST00000698451.1:n.2212C=
ENST00000698452.1:n.3283C=
ENST00000698453.1:c.2468C= ENSP00000513735.1:p.Ala823=
ENST00000698454.1:c.2533C= ENSP00000513736.1:p.His845=
ENST00000698455.1:c.*2768C= ENSP00000513737.1:n.*2768C=
ENST00000698456.1:c.*1400C= ENSP00000513738.1:n.*1400C=
ENST00000698457.1:c.2332C= ENSP00000513739.1:p.His778=
ENST00000698458.1:c.2504C= ENSP00000513740.1:p.Ala835=
ENST00000698459.1:c.2542C= ENSP00000513741.1:p.His848=
ENST00000698460.1:c.*305C= ENSP00000513742.1:n.*305C=
ENST00000698461.1:n.2997C=
ENST00000698462.1:n.2917C=
ENST00000698468.1:n.3283C=
ENST00000698469.1:c.*2139C= ENSP00000513743.1:n.*2139C=
ENST00000698470.1:c.*634C= ENSP00000513744.1:n.*634C=
ENST00000698471.1:n.3082C=
ENST00000698472.1:c.*1507C= ENSP00000513745.1:n.*1507C=
ENST00000698473.1:n.3082C=
ENST00000698474.1:n.3082C=
ENST00000698475.1:n.3167C=
ENST00000698476.1:c.2542C= ENSP00000513746.1:p.His848=
ENST00000698477.1:c.2468C= ENSP00000513747.1:p.Ala823=
ENST00000698478.1:n.3082C=
ENST00000698479.1:c.2542C= ENSP00000513748.1:p.His848=
ENST00000698480.1:c.2463C= ENSP00000513749.1:p.Ser821=
ENST00000698481.1:c.2463C= ENSP00000513750.1:p.Ser821=
ENST00000698482.1:n.2832C=
ENST00000698483.1:n.2997C=
ENST00000698484.1:c.2542C= ENSP00000513751.1:p.His848=
ENST00000698485.1:c.2463C= ENSP00000513752.1:p.Ser821=
ENST00000698486.1:n.3082C=
ENST00000698487.1:c.2542C= ENSP00000513753.1:p.His848=
ENST00000698488.1:c.2286C= ENSP00000513754.1:p.Ser762=
ENST00000698489.1:n.6867C=
ENST00000698490.1:c.2542C= ENSP00000513755.1:p.His848=
ENST00000698492.1:c.*1257C= ENSP00000513756.1:n.*1257C=
ENST00000698493.1:n.2832C=
ENST00000698494.1:c.*522C= ENSP00000513757.1:n.*522C=
ENST00000358746.7:c.2542C= MANE Select ENSP00000351596.3:p.His848=
ENST00000649566.1:c.2542C= ENSP00000497948.1:p.His848=
ENST00000358746.6:c.2542C= ENSP00000351596.2:p.His848=
ENST00000506007.1:n.209C=
ENST00000507805.5:n.814C=
ENST00000508181.5:n.115C=
NM_014639.3:c.2542C= , LRG_173t1:c.2542C= NP_055454.1:p.His848=
XR_948312.1:n.2811C=
XR_001742370.2:n.2814C=
NM_014639.4:c.2542C= MANE Select NP_055454.1:p.His848=