Canonical Allele Identifier: CA1565024349
Gene: SKIC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516568A= , CM000667.2:g.95516568A= GRCh38
NC_000005.9:g.94852272A= , CM000667.1:g.94852272A= GRCh37
NC_000005.8:g.94878028A= NCBI36
NG_023414.1:g.43438T= , LRG_173:g.43438T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000506007.2:n.3074T=
ENST00000513232.2:c.*1499T= ENSP00000422749.2:n.*1499T=
ENST00000698450.1:n.1918T=
ENST00000698451.1:n.2204T=
ENST00000698452.1:n.3275T=
ENST00000698453.1:c.2460T= ENSP00000513735.1:p.Pro820=
ENST00000698454.1:c.2525T= ENSP00000513736.1:p.Leu842=
ENST00000698455.1:c.*2760T= ENSP00000513737.1:n.*2760T=
ENST00000698456.1:c.*1392T= ENSP00000513738.1:n.*1392T=
ENST00000698457.1:c.2324T= ENSP00000513739.1:p.Leu775=
ENST00000698458.1:c.2496T= ENSP00000513740.1:p.Pro832=
ENST00000698459.1:c.2534T= ENSP00000513741.1:p.Leu845=
ENST00000698460.1:c.*297T= ENSP00000513742.1:n.*297T=
ENST00000698461.1:n.2989T=
ENST00000698462.1:n.2909T=
ENST00000698468.1:n.3275T=
ENST00000698469.1:c.*2131T= ENSP00000513743.1:n.*2131T=
ENST00000698470.1:c.*626T= ENSP00000513744.1:n.*626T=
ENST00000698471.1:n.3074T=
ENST00000698472.1:c.*1499T= ENSP00000513745.1:n.*1499T=
ENST00000698473.1:n.3074T=
ENST00000698474.1:n.3074T=
ENST00000698475.1:n.3159T=
ENST00000698476.1:c.2534T= ENSP00000513746.1:p.Leu845=
ENST00000698477.1:c.2460T= ENSP00000513747.1:p.Pro820=
ENST00000698478.1:n.3074T=
ENST00000698479.1:c.2534T= ENSP00000513748.1:p.Leu845=
ENST00000698480.1:c.2455T= ENSP00000513749.1:p.Leu819=
ENST00000698481.1:c.2455T= ENSP00000513750.1:p.Leu819=
ENST00000698482.1:n.2824T=
ENST00000698483.1:n.2989T=
ENST00000698484.1:c.2534T= ENSP00000513751.1:p.Leu845=
ENST00000698485.1:c.2455T= ENSP00000513752.1:p.Leu819=
ENST00000698486.1:n.3074T=
ENST00000698487.1:c.2534T= ENSP00000513753.1:p.Leu845=
ENST00000698488.1:c.2278T= ENSP00000513754.1:p.Leu760=
ENST00000698489.1:n.6859T=
ENST00000698490.1:c.2534T= ENSP00000513755.1:p.Leu845=
ENST00000698492.1:c.*1249T= ENSP00000513756.1:n.*1249T=
ENST00000698493.1:n.2824T=
ENST00000698494.1:c.*514T= ENSP00000513757.1:n.*514T=
ENST00000358746.7:c.2534T= MANE Select ENSP00000351596.3:p.Leu845=
ENST00000649566.1:c.2534T= ENSP00000497948.1:p.Leu845=
ENST00000358746.6:c.2534T= ENSP00000351596.2:p.Leu845=
ENST00000506007.1:n.201T=
ENST00000507805.5:n.806T=
ENST00000508181.5:n.107T=
NM_014639.3:c.2534T= , LRG_173t1:c.2534T= NP_055454.1:p.Leu845=
XR_948312.1:n.2803T=
XR_001742370.2:n.2806T=
NM_014639.4:c.2534T= MANE Select NP_055454.1:p.Leu845=