Canonical Allele Identifier: CA360457855
Gene: SKIC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516573A>T , CM000667.2:g.95516573A>T GRCh38
NC_000005.9:g.94852277A>T , CM000667.1:g.94852277A>T GRCh37
NC_000005.8:g.94878033A>T NCBI36
NG_023414.1:g.43433T>A , LRG_173:g.43433T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000506007.2:n.3069T>A
ENST00000513232.2:c.*1494T>A ENSP00000422749.2:n.*1494T>A
ENST00000698450.1:n.1913T>A
ENST00000698451.1:n.2199T>A
ENST00000698452.1:n.3270T>A
ENST00000698453.1:c.2455T>A ENSP00000513735.1:p.Cys819Ser
ENST00000698454.1:c.2520T>A ENSP00000513736.1:p.Tyr840Ter
ENST00000698455.1:c.*2755T>A ENSP00000513737.1:n.*2755T>A
ENST00000698456.1:c.*1387T>A ENSP00000513738.1:n.*1387T>A
ENST00000698457.1:c.2319T>A ENSP00000513739.1:p.Tyr773Ter
ENST00000698458.1:c.2491T>A ENSP00000513740.1:p.Cys831Ser
ENST00000698459.1:c.2529T>A ENSP00000513741.1:p.Tyr843Ter
ENST00000698460.1:c.*292T>A ENSP00000513742.1:n.*292T>A
ENST00000698461.1:n.2984T>A
ENST00000698462.1:n.2904T>A
ENST00000698468.1:n.3270T>A
ENST00000698469.1:c.*2126T>A ENSP00000513743.1:n.*2126T>A
ENST00000698470.1:c.*621T>A ENSP00000513744.1:n.*621T>A
ENST00000698471.1:n.3069T>A
ENST00000698472.1:c.*1494T>A ENSP00000513745.1:n.*1494T>A
ENST00000698473.1:n.3069T>A
ENST00000698474.1:n.3069T>A
ENST00000698475.1:n.3154T>A
ENST00000698476.1:c.2529T>A ENSP00000513746.1:p.Tyr843Ter
ENST00000698477.1:c.2455T>A ENSP00000513747.1:p.Cys819Ser
ENST00000698478.1:n.3069T>A
ENST00000698479.1:c.2529T>A ENSP00000513748.1:p.Tyr843Ter
ENST00000698480.1:c.2450T>A ENSP00000513749.1:p.Met817Lys
ENST00000698481.1:c.2450T>A ENSP00000513750.1:p.Met817Lys
ENST00000698482.1:n.2819T>A
ENST00000698483.1:n.2984T>A
ENST00000698484.1:c.2529T>A ENSP00000513751.1:p.Tyr843Ter
ENST00000698485.1:c.2450T>A ENSP00000513752.1:p.Met817Lys
ENST00000698486.1:n.3069T>A
ENST00000698487.1:c.2529T>A ENSP00000513753.1:p.Tyr843Ter
ENST00000698488.1:c.2273T>A ENSP00000513754.1:p.Met758Lys
ENST00000698489.1:n.6854T>A
ENST00000698490.1:c.2529T>A ENSP00000513755.1:p.Tyr843Ter
ENST00000698492.1:c.*1244T>A ENSP00000513756.1:n.*1244T>A
ENST00000698493.1:n.2819T>A
ENST00000698494.1:c.*509T>A ENSP00000513757.1:n.*509T>A
ENST00000358746.7:c.2529T>A MANE Select ENSP00000351596.3:p.Tyr843Ter
ENST00000649566.1:c.2529T>A ENSP00000497948.1:p.Tyr843Ter
ENST00000358746.6:c.2529T>A ENSP00000351596.2:p.Tyr843Ter
ENST00000506007.1:n.196T>A
ENST00000507805.5:n.801T>A
ENST00000508181.5:n.102T>A
NM_014639.3:c.2529T>A , LRG_173t1:c.2529T>A NP_055454.1:p.Tyr843Ter
XR_948312.1:n.2798T>A
XR_001742370.2:n.2801T>A
NM_014639.4:c.2529T>A MANE Select NP_055454.1:p.Tyr843Ter