Canonical Allele Identifier: CA360458425
Gene: SKIC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516730T>A , CM000667.2:g.95516730T>A GRCh38
NC_000005.9:g.94852434T>A , CM000667.1:g.94852434T>A GRCh37
NC_000005.8:g.94878190T>A NCBI36
NG_023414.1:g.43276A>T , LRG_173:g.43276A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000506007.2:n.2912A>T
ENST00000513232.2:c.*1337A>T ENSP00000422749.2:n.*1337A>T
ENST00000698450.1:n.1841A>T
ENST00000698451.1:n.2042A>T
ENST00000698452.1:n.3113A>T
ENST00000698453.1:c.2442-144A>T ENSP00000513735.1:n.2442-144A>T
ENST00000698454.1:c.2448A>T ENSP00000513736.1:p.Arg816Ser
ENST00000698455.1:c.*2598A>T ENSP00000513737.1:n.*2598A>T
ENST00000698456.1:c.*1315A>T ENSP00000513738.1:n.*1315A>T
ENST00000698457.1:c.2247A>T ENSP00000513739.1:p.Arg749Ser
ENST00000698458.1:c.2478-144A>T ENSP00000513740.1:n.2478-144A>T
ENST00000698459.1:c.2457A>T ENSP00000513741.1:p.Arg819Ser
ENST00000698460.1:c.*279-144A>T ENSP00000513742.1:n.*279-144A>T
ENST00000698461.1:n.2912A>T
ENST00000698462.1:n.2832A>T
ENST00000698468.1:n.3113A>T
ENST00000698469.1:c.*1969A>T ENSP00000513743.1:n.*1969A>T
ENST00000698470.1:c.*464A>T ENSP00000513744.1:n.*464A>T
ENST00000698471.1:n.2912A>T
ENST00000698472.1:c.*1337A>T ENSP00000513745.1:n.*1337A>T
ENST00000698473.1:n.2912A>T
ENST00000698474.1:n.2912A>T
ENST00000698475.1:n.2997A>T
ENST00000698476.1:c.2457A>T ENSP00000513746.1:p.Arg819Ser
ENST00000698477.1:c.2442-144A>T ENSP00000513747.1:n.2442-144A>T
ENST00000698478.1:n.2912A>T
ENST00000698479.1:c.2457A>T ENSP00000513748.1:p.Arg819Ser
ENST00000698480.1:c.2437-144A>T ENSP00000513749.1:n.2437-144A>T
ENST00000698481.1:c.2437-144A>T ENSP00000513750.1:n.2437-144A>T
ENST00000698482.1:n.2747A>T
ENST00000698483.1:n.2912A>T
ENST00000698484.1:c.2457A>T ENSP00000513751.1:p.Arg819Ser
ENST00000698485.1:c.2437-144A>T ENSP00000513752.1:n.2437-144A>T
ENST00000698486.1:n.2912A>T
ENST00000698487.1:c.2457A>T ENSP00000513753.1:p.Arg819Ser
ENST00000698488.1:c.2260-144A>T ENSP00000513754.1:n.2260-144A>T
ENST00000698489.1:n.6697A>T
ENST00000698490.1:c.2457A>T ENSP00000513755.1:p.Arg819Ser
ENST00000698492.1:c.*1172A>T ENSP00000513756.1:n.*1172A>T
ENST00000698493.1:n.2747A>T
ENST00000698494.1:c.*352A>T ENSP00000513757.1:n.*352A>T
ENST00000358746.7:c.2457A>T MANE Select ENSP00000351596.3:p.Arg819Ser
ENST00000649566.1:c.2457A>T ENSP00000497948.1:p.Arg819Ser
ENST00000358746.6:c.2457A>T ENSP00000351596.2:p.Arg819Ser
ENST00000506007.1:n.39A>T
ENST00000507805.5:n.644A>T
NM_014639.3:c.2457A>T , LRG_173t1:c.2457A>T NP_055454.1:p.Arg819Ser
XR_948312.1:n.2726A>T
XR_001742370.2:n.2729A>T
NM_014639.4:c.2457A>T MANE Select NP_055454.1:p.Arg819Ser