Canonical Allele Identifier: CA360458600
Gene: SKIC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516746A>G , CM000667.2:g.95516746A>G GRCh38
NC_000005.9:g.94852450A>G , CM000667.1:g.94852450A>G GRCh37
NC_000005.8:g.94878206A>G NCBI36
NG_023414.1:g.43260T>C , LRG_173:g.43260T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000506007.2:n.2896T>C
ENST00000513232.2:c.*1321T>C ENSP00000422749.2:n.*1321T>C
ENST00000698450.1:n.1825T>C
ENST00000698451.1:n.2026T>C
ENST00000698452.1:n.3097T>C
ENST00000698453.1:c.2442-160T>C ENSP00000513735.1:n.2442-160T>C
ENST00000698454.1:c.2432T>C ENSP00000513736.1:p.Leu811Pro
ENST00000698455.1:c.*2582T>C ENSP00000513737.1:n.*2582T>C
ENST00000698456.1:c.*1299T>C ENSP00000513738.1:n.*1299T>C
ENST00000698457.1:c.2231T>C ENSP00000513739.1:p.Leu744Pro
ENST00000698458.1:c.2478-160T>C ENSP00000513740.1:n.2478-160T>C
ENST00000698459.1:c.2441T>C ENSP00000513741.1:p.Leu814Pro
ENST00000698460.1:c.*279-160T>C ENSP00000513742.1:n.*279-160T>C
ENST00000698461.1:n.2896T>C
ENST00000698462.1:n.2816T>C
ENST00000698468.1:n.3097T>C
ENST00000698469.1:c.*1953T>C ENSP00000513743.1:n.*1953T>C
ENST00000698470.1:c.*448T>C ENSP00000513744.1:n.*448T>C
ENST00000698471.1:n.2896T>C
ENST00000698472.1:c.*1321T>C ENSP00000513745.1:n.*1321T>C
ENST00000698473.1:n.2896T>C
ENST00000698474.1:n.2896T>C
ENST00000698475.1:n.2981T>C
ENST00000698476.1:c.2441T>C ENSP00000513746.1:p.Leu814Pro
ENST00000698477.1:c.2442-160T>C ENSP00000513747.1:n.2442-160T>C
ENST00000698478.1:n.2896T>C
ENST00000698479.1:c.2441T>C ENSP00000513748.1:p.Leu814Pro
ENST00000698480.1:c.2437-160T>C ENSP00000513749.1:n.2437-160T>C
ENST00000698481.1:c.2437-160T>C ENSP00000513750.1:n.2437-160T>C
ENST00000698482.1:n.2731T>C
ENST00000698483.1:n.2896T>C
ENST00000698484.1:c.2441T>C ENSP00000513751.1:p.Leu814Pro
ENST00000698485.1:c.2437-160T>C ENSP00000513752.1:n.2437-160T>C
ENST00000698486.1:n.2896T>C
ENST00000698487.1:c.2441T>C ENSP00000513753.1:p.Leu814Pro
ENST00000698488.1:c.2260-160T>C ENSP00000513754.1:n.2260-160T>C
ENST00000698489.1:n.6681T>C
ENST00000698490.1:c.2441T>C ENSP00000513755.1:p.Leu814Pro
ENST00000698492.1:c.*1156T>C ENSP00000513756.1:n.*1156T>C
ENST00000698493.1:n.2731T>C
ENST00000698494.1:c.*336T>C ENSP00000513757.1:n.*336T>C
ENST00000358746.7:c.2441T>C MANE Select ENSP00000351596.3:p.Leu814Pro
ENST00000649566.1:c.2441T>C ENSP00000497948.1:p.Leu814Pro
ENST00000358746.6:c.2441T>C ENSP00000351596.2:p.Leu814Pro
ENST00000506007.1:n.23T>C
ENST00000507805.5:n.628T>C
NM_014639.3:c.2441T>C , LRG_173t1:c.2441T>C NP_055454.1:p.Leu814Pro
XR_948312.1:n.2710T>C
XR_001742370.2:n.2713T>C
NM_014639.4:c.2441T>C MANE Select NP_055454.1:p.Leu814Pro