Canonical Allele Identifier: CA1565024343
Gene: SKIC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516557A= , CM000667.2:g.95516557A= GRCh38
NC_000005.9:g.94852261A= , CM000667.1:g.94852261A= GRCh37
NC_000005.8:g.94878017A= NCBI36
NG_023414.1:g.43449T= , LRG_173:g.43449T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000506007.2:n.3085T=
ENST00000513232.2:c.*1510T= ENSP00000422749.2:n.*1510T=
ENST00000698450.1:n.1929T=
ENST00000698451.1:n.2215T=
ENST00000698452.1:n.3286T=
ENST00000698453.1:c.2471T= ENSP00000513735.1:p.Leu824=
ENST00000698454.1:c.2536T= ENSP00000513736.1:p.Cys846=
ENST00000698455.1:c.*2771T= ENSP00000513737.1:n.*2771T=
ENST00000698456.1:c.*1403T= ENSP00000513738.1:n.*1403T=
ENST00000698457.1:c.2335T= ENSP00000513739.1:p.Cys779=
ENST00000698458.1:c.2507T= ENSP00000513740.1:p.Leu836=
ENST00000698459.1:c.2545T= ENSP00000513741.1:p.Cys849=
ENST00000698460.1:c.*308T= ENSP00000513742.1:n.*308T=
ENST00000698461.1:n.3000T=
ENST00000698462.1:n.2920T=
ENST00000698468.1:n.3286T=
ENST00000698469.1:c.*2142T= ENSP00000513743.1:n.*2142T=
ENST00000698470.1:c.*637T= ENSP00000513744.1:n.*637T=
ENST00000698471.1:n.3085T=
ENST00000698472.1:c.*1510T= ENSP00000513745.1:n.*1510T=
ENST00000698473.1:n.3085T=
ENST00000698474.1:n.3085T=
ENST00000698475.1:n.3170T=
ENST00000698476.1:c.2545T= ENSP00000513746.1:p.Cys849=
ENST00000698477.1:c.2471T= ENSP00000513747.1:p.Leu824=
ENST00000698478.1:n.3085T=
ENST00000698479.1:c.2545T= ENSP00000513748.1:p.Cys849=
ENST00000698480.1:c.2466T= ENSP00000513749.1:p.Thr822=
ENST00000698481.1:c.2466T= ENSP00000513750.1:p.Thr822=
ENST00000698482.1:n.2835T=
ENST00000698483.1:n.3000T=
ENST00000698484.1:c.2545T= ENSP00000513751.1:p.Cys849=
ENST00000698485.1:c.2466T= ENSP00000513752.1:p.Thr822=
ENST00000698486.1:n.3085T=
ENST00000698487.1:c.2545T= ENSP00000513753.1:p.Cys849=
ENST00000698488.1:c.2289T= ENSP00000513754.1:p.Thr763=
ENST00000698489.1:n.6870T=
ENST00000698490.1:c.2545T= ENSP00000513755.1:p.Cys849=
ENST00000698492.1:c.*1260T= ENSP00000513756.1:n.*1260T=
ENST00000698493.1:n.2835T=
ENST00000698494.1:c.*525T= ENSP00000513757.1:n.*525T=
ENST00000358746.7:c.2545T= MANE Select ENSP00000351596.3:p.Cys849=
ENST00000649566.1:c.2545T= ENSP00000497948.1:p.Cys849=
ENST00000358746.6:c.2545T= ENSP00000351596.2:p.Cys849=
ENST00000506007.1:n.212T=
ENST00000507805.5:n.817T=
ENST00000508181.5:n.118T=
NM_014639.3:c.2545T= , LRG_173t1:c.2545T= NP_055454.1:p.Cys849=
XR_948312.1:n.2814T=
XR_001742370.2:n.2817T=
NM_014639.4:c.2545T= MANE Select NP_055454.1:p.Cys849=