Canonical Allele Identifier: CA360458416
Gene: SKIC3 HGNC NCBI

Linked Data

dbSNP Id: rs1747316059

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516729G>A , CM000667.2:g.95516729G>A GRCh38
NC_000005.9:g.94852433G>A , CM000667.1:g.94852433G>A GRCh37
NC_000005.8:g.94878189G>A NCBI36
NG_023414.1:g.43277C>T , LRG_173:g.43277C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000506007.2:n.2913C>T
ENST00000513232.2:c.*1338C>T ENSP00000422749.2:n.*1338C>T
ENST00000698450.1:n.1842C>T
ENST00000698451.1:n.2043C>T
ENST00000698452.1:n.3114C>T
ENST00000698453.1:c.2442-143C>T ENSP00000513735.1:n.2442-143C>T
ENST00000698454.1:c.2449C>T ENSP00000513736.1:p.Leu817Phe
ENST00000698455.1:c.*2599C>T ENSP00000513737.1:n.*2599C>T
ENST00000698456.1:c.*1316C>T ENSP00000513738.1:n.*1316C>T
ENST00000698457.1:c.2248C>T ENSP00000513739.1:p.Leu750Phe
ENST00000698458.1:c.2478-143C>T ENSP00000513740.1:n.2478-143C>T
ENST00000698459.1:c.2458C>T ENSP00000513741.1:p.Leu820Phe
ENST00000698460.1:c.*279-143C>T ENSP00000513742.1:n.*279-143C>T
ENST00000698461.1:n.2913C>T
ENST00000698462.1:n.2833C>T
ENST00000698468.1:n.3114C>T
ENST00000698469.1:c.*1970C>T ENSP00000513743.1:n.*1970C>T
ENST00000698470.1:c.*465C>T ENSP00000513744.1:n.*465C>T
ENST00000698471.1:n.2913C>T
ENST00000698472.1:c.*1338C>T ENSP00000513745.1:n.*1338C>T
ENST00000698473.1:n.2913C>T
ENST00000698474.1:n.2913C>T
ENST00000698475.1:n.2998C>T
ENST00000698476.1:c.2458C>T ENSP00000513746.1:p.Leu820Phe
ENST00000698477.1:c.2442-143C>T ENSP00000513747.1:n.2442-143C>T
ENST00000698478.1:n.2913C>T
ENST00000698479.1:c.2458C>T ENSP00000513748.1:p.Leu820Phe
ENST00000698480.1:c.2437-143C>T ENSP00000513749.1:n.2437-143C>T
ENST00000698481.1:c.2437-143C>T ENSP00000513750.1:n.2437-143C>T
ENST00000698482.1:n.2748C>T
ENST00000698483.1:n.2913C>T
ENST00000698484.1:c.2458C>T ENSP00000513751.1:p.Leu820Phe
ENST00000698485.1:c.2437-143C>T ENSP00000513752.1:n.2437-143C>T
ENST00000698486.1:n.2913C>T
ENST00000698487.1:c.2458C>T ENSP00000513753.1:p.Leu820Phe
ENST00000698488.1:c.2260-143C>T ENSP00000513754.1:n.2260-143C>T
ENST00000698489.1:n.6698C>T
ENST00000698490.1:c.2458C>T ENSP00000513755.1:p.Leu820Phe
ENST00000698492.1:c.*1173C>T ENSP00000513756.1:n.*1173C>T
ENST00000698493.1:n.2748C>T
ENST00000698494.1:c.*353C>T ENSP00000513757.1:n.*353C>T
ENST00000358746.7:c.2458C>T MANE Select ENSP00000351596.3:p.Leu820Phe
ENST00000649566.1:c.2458C>T ENSP00000497948.1:p.Leu820Phe
ENST00000358746.6:c.2458C>T ENSP00000351596.2:p.Leu820Phe
ENST00000506007.1:n.40C>T
ENST00000507805.5:n.645C>T
NM_014639.3:c.2458C>T , LRG_173t1:c.2458C>T NP_055454.1:p.Leu820Phe
XR_948312.1:n.2727C>T
XR_001742370.2:n.2730C>T
NM_014639.4:c.2458C>T MANE Select NP_055454.1:p.Leu820Phe