Canonical Allele Identifier: CA1565027208
Gene: SKIC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95523669C= , CM000667.2:g.95523669C= GRCh38
NC_000005.9:g.94859373C= , CM000667.1:g.94859373C= GRCh37
NC_000005.8:g.94885129C= NCBI36
NG_023414.1:g.36337G= , LRG_173:g.36337G=

Transcript Alleles

HGVS Amino-acid change
ENST00000506007.2:n.1908G=
ENST00000513232.2:c.*333G= ENSP00000422749.2:n.*333G=
ENST00000698450.1:n.1002G=
ENST00000698451.1:n.1038G=
ENST00000698452.1:n.2109G=
ENST00000698453.1:c.1618G= ENSP00000513735.1:p.Glu540=
ENST00000698454.1:c.1609G= ENSP00000513736.1:p.Glu537=
ENST00000698455.1:c.*1594G= ENSP00000513737.1:n.*1594G=
ENST00000698456.1:c.*476G= ENSP00000513738.1:n.*476G=
ENST00000698457.1:c.1618G= ENSP00000513739.1:p.Glu540=
ENST00000698458.1:c.1654G= ENSP00000513740.1:p.Glu552=
ENST00000698459.1:c.1618G= ENSP00000513741.1:p.Glu540=
ENST00000698460.1:c.1618G= ENSP00000513742.1:p.Glu540=
ENST00000698461.1:n.1908G=
ENST00000698462.1:n.1908G=
ENST00000698468.1:n.2109G=
ENST00000698469.1:c.*965G= ENSP00000513743.1:n.*965G=
ENST00000698470.1:c.1618G= ENSP00000513744.1:p.Glu540=
ENST00000698471.1:n.1908G=
ENST00000698472.1:c.*333G= ENSP00000513745.1:n.*333G=
ENST00000698473.1:n.1908G=
ENST00000698474.1:n.1908G=
ENST00000698475.1:n.1908G=
ENST00000698476.1:c.1618G= ENSP00000513746.1:p.Glu540=
ENST00000698477.1:c.1618G= ENSP00000513747.1:p.Glu540=
ENST00000698478.1:n.1908G=
ENST00000698479.1:c.1618G= ENSP00000513748.1:p.Glu540=
ENST00000698480.1:c.1618G= ENSP00000513749.1:p.Glu540=
ENST00000698481.1:c.1618G= ENSP00000513750.1:p.Glu540=
ENST00000698482.1:n.1908G=
ENST00000698483.1:n.1908G=
ENST00000698484.1:c.1618G= ENSP00000513751.1:p.Glu540=
ENST00000698485.1:c.1618G= ENSP00000513752.1:p.Glu540=
ENST00000698486.1:n.1908G=
ENST00000698487.1:c.1618G= ENSP00000513753.1:p.Glu540=
ENST00000698488.1:c.1618G= ENSP00000513754.1:p.Glu540=
ENST00000698489.1:n.5693G=
ENST00000698490.1:c.1618G= ENSP00000513755.1:p.Glu540=
ENST00000698492.1:c.*333G= ENSP00000513756.1:n.*333G=
ENST00000698493.1:n.1908G=
ENST00000698494.1:c.1618G= ENSP00000513757.1:p.Glu540=
ENST00000358746.7:c.1618G= MANE Select ENSP00000351596.3:p.Glu540=
ENST00000649566.1:c.1618G= ENSP00000497948.1:p.Glu540=
ENST00000358746.6:c.1618G= ENSP00000351596.2:p.Glu540=
ENST00000505578.5:c.320-343G= ENSP00000423141.1:n.320-343G=
ENST00000513232.1:c.435G= ENSP00000422749.1:n.435G=
ENST00000514952.5:c.1474G= ENSP00000423742.1:p.Glu492=
NM_014639.3:c.1618G= , LRG_173t1:c.1618G= NP_055454.1:p.Glu540=
XR_948312.1:n.1887G=
XR_001742370.2:n.1890G=
NM_014639.4:c.1618G= MANE Select NP_055454.1:p.Glu540=