Canonical Allele Identifier: CA1565024355
Gene: SKIC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516584T= , CM000667.2:g.95516584T= GRCh38
NC_000005.9:g.94852288T= , CM000667.1:g.94852288T= GRCh37
NC_000005.8:g.94878044T= NCBI36
NG_023414.1:g.43422A= , LRG_173:g.43422A=

Transcript Alleles

HGVS Amino-acid change
ENST00000506007.2:n.3058A=
ENST00000513232.2:c.*1483A= ENSP00000422749.2:n.*1483A=
ENST00000698450.1:n.1902A=
ENST00000698451.1:n.2188A=
ENST00000698452.1:n.3259A=
ENST00000698453.1:c.2444A= ENSP00000513735.1:p.Tyr815=
ENST00000698454.1:c.2509A= ENSP00000513736.1:p.Ile837=
ENST00000698455.1:c.*2744A= ENSP00000513737.1:n.*2744A=
ENST00000698456.1:c.*1376A= ENSP00000513738.1:n.*1376A=
ENST00000698457.1:c.2308A= ENSP00000513739.1:p.Ile770=
ENST00000698458.1:c.2480A= ENSP00000513740.1:p.Tyr827=
ENST00000698459.1:c.2518A= ENSP00000513741.1:p.Ile840=
ENST00000698460.1:c.*281A= ENSP00000513742.1:n.*281A=
ENST00000698461.1:n.2973A=
ENST00000698462.1:n.2893A=
ENST00000698468.1:n.3259A=
ENST00000698469.1:c.*2115A= ENSP00000513743.1:n.*2115A=
ENST00000698470.1:c.*610A= ENSP00000513744.1:n.*610A=
ENST00000698471.1:n.3058A=
ENST00000698472.1:c.*1483A= ENSP00000513745.1:n.*1483A=
ENST00000698473.1:n.3058A=
ENST00000698474.1:n.3058A=
ENST00000698475.1:n.3143A=
ENST00000698476.1:c.2518A= ENSP00000513746.1:p.Ile840=
ENST00000698477.1:c.2444A= ENSP00000513747.1:p.Tyr815=
ENST00000698478.1:n.3058A=
ENST00000698479.1:c.2518A= ENSP00000513748.1:p.Ile840=
ENST00000698480.1:c.2439A= ENSP00000513749.1:p.Val813=
ENST00000698481.1:c.2439A= ENSP00000513750.1:p.Val813=
ENST00000698482.1:n.2808A=
ENST00000698483.1:n.2973A=
ENST00000698484.1:c.2518A= ENSP00000513751.1:p.Ile840=
ENST00000698485.1:c.2439A= ENSP00000513752.1:p.Val813=
ENST00000698486.1:n.3058A=
ENST00000698487.1:c.2518A= ENSP00000513753.1:p.Ile840=
ENST00000698488.1:c.2262A= ENSP00000513754.1:p.Val754=
ENST00000698489.1:n.6843A=
ENST00000698490.1:c.2518A= ENSP00000513755.1:p.Ile840=
ENST00000698492.1:c.*1233A= ENSP00000513756.1:n.*1233A=
ENST00000698493.1:n.2808A=
ENST00000698494.1:c.*498A= ENSP00000513757.1:n.*498A=
ENST00000358746.7:c.2518A= MANE Select ENSP00000351596.3:p.Ile840=
ENST00000649566.1:c.2518A= ENSP00000497948.1:p.Ile840=
ENST00000358746.6:c.2518A= ENSP00000351596.2:p.Ile840=
ENST00000506007.1:n.185A=
ENST00000507805.5:n.790A=
ENST00000508181.5:n.91A=
NM_014639.3:c.2518A= , LRG_173t1:c.2518A= NP_055454.1:p.Ile840=
XR_948312.1:n.2787A=
XR_001742370.2:n.2790A=
NM_014639.4:c.2518A= MANE Select NP_055454.1:p.Ile840=