Canonical Allele Identifier: CA1565024419
Gene: SKIC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516721A= , CM000667.2:g.95516721A= GRCh38
NC_000005.9:g.94852425A= , CM000667.1:g.94852425A= GRCh37
NC_000005.8:g.94878181A= NCBI36
NG_023414.1:g.43285T= , LRG_173:g.43285T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000506007.2:n.2921T=
ENST00000513232.2:c.*1346T= ENSP00000422749.2:n.*1346T=
ENST00000698450.1:n.1850T=
ENST00000698451.1:n.2051T=
ENST00000698452.1:n.3122T=
ENST00000698453.1:c.2442-135T= ENSP00000513735.1:n.2442-135T=
ENST00000698454.1:c.2457T= ENSP00000513736.1:p.Ser819=
ENST00000698455.1:c.*2607T= ENSP00000513737.1:n.*2607T=
ENST00000698456.1:c.*1324T= ENSP00000513738.1:n.*1324T=
ENST00000698457.1:c.2256T= ENSP00000513739.1:p.Ser752=
ENST00000698458.1:c.2478-135T= ENSP00000513740.1:n.2478-135T=
ENST00000698459.1:c.2466T= ENSP00000513741.1:p.Ser822=
ENST00000698460.1:c.*279-135T= ENSP00000513742.1:n.*279-135T=
ENST00000698461.1:n.2921T=
ENST00000698462.1:n.2841T=
ENST00000698468.1:n.3122T=
ENST00000698469.1:c.*1978T= ENSP00000513743.1:n.*1978T=
ENST00000698470.1:c.*473T= ENSP00000513744.1:n.*473T=
ENST00000698471.1:n.2921T=
ENST00000698472.1:c.*1346T= ENSP00000513745.1:n.*1346T=
ENST00000698473.1:n.2921T=
ENST00000698474.1:n.2921T=
ENST00000698475.1:n.3006T=
ENST00000698476.1:c.2466T= ENSP00000513746.1:p.Ser822=
ENST00000698477.1:c.2442-135T= ENSP00000513747.1:n.2442-135T=
ENST00000698478.1:n.2921T=
ENST00000698479.1:c.2466T= ENSP00000513748.1:p.Ser822=
ENST00000698480.1:c.2437-135T= ENSP00000513749.1:n.2437-135T=
ENST00000698481.1:c.2437-135T= ENSP00000513750.1:n.2437-135T=
ENST00000698482.1:n.2756T=
ENST00000698483.1:n.2921T=
ENST00000698484.1:c.2466T= ENSP00000513751.1:p.Ser822=
ENST00000698485.1:c.2437-135T= ENSP00000513752.1:n.2437-135T=
ENST00000698486.1:n.2921T=
ENST00000698487.1:c.2466T= ENSP00000513753.1:p.Ser822=
ENST00000698488.1:c.2260-135T= ENSP00000513754.1:n.2260-135T=
ENST00000698489.1:n.6706T=
ENST00000698490.1:c.2466T= ENSP00000513755.1:p.Ser822=
ENST00000698492.1:c.*1181T= ENSP00000513756.1:n.*1181T=
ENST00000698493.1:n.2756T=
ENST00000698494.1:c.*361T= ENSP00000513757.1:n.*361T=
ENST00000358746.7:c.2466T= MANE Select ENSP00000351596.3:p.Ser822=
ENST00000649566.1:c.2466T= ENSP00000497948.1:p.Ser822=
ENST00000358746.6:c.2466T= ENSP00000351596.2:p.Ser822=
ENST00000506007.1:n.48T=
ENST00000507805.5:n.653T=
NM_014639.3:c.2466T= , LRG_173t1:c.2466T= NP_055454.1:p.Ser822=
XR_948312.1:n.2735T=
XR_001742370.2:n.2738T=
NM_014639.4:c.2466T= MANE Select NP_055454.1:p.Ser822=