Canonical Allele Identifier: CA1565024352
Gene: SKIC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516578T= , CM000667.2:g.95516578T= GRCh38
NC_000005.9:g.94852282T= , CM000667.1:g.94852282T= GRCh37
NC_000005.8:g.94878038T= NCBI36
NG_023414.1:g.43428A= , LRG_173:g.43428A=

Transcript Alleles

HGVS Amino-acid change
ENST00000506007.2:n.3064A=
ENST00000513232.2:c.*1489A= ENSP00000422749.2:n.*1489A=
ENST00000698450.1:n.1908A=
ENST00000698451.1:n.2194A=
ENST00000698452.1:n.3265A=
ENST00000698453.1:c.2450A= ENSP00000513735.1:p.Lys817=
ENST00000698454.1:c.2515A= ENSP00000513736.1:p.Asn839=
ENST00000698455.1:c.*2750A= ENSP00000513737.1:n.*2750A=
ENST00000698456.1:c.*1382A= ENSP00000513738.1:n.*1382A=
ENST00000698457.1:c.2314A= ENSP00000513739.1:p.Asn772=
ENST00000698458.1:c.2486A= ENSP00000513740.1:p.Lys829=
ENST00000698459.1:c.2524A= ENSP00000513741.1:p.Asn842=
ENST00000698460.1:c.*287A= ENSP00000513742.1:n.*287A=
ENST00000698461.1:n.2979A=
ENST00000698462.1:n.2899A=
ENST00000698468.1:n.3265A=
ENST00000698469.1:c.*2121A= ENSP00000513743.1:n.*2121A=
ENST00000698470.1:c.*616A= ENSP00000513744.1:n.*616A=
ENST00000698471.1:n.3064A=
ENST00000698472.1:c.*1489A= ENSP00000513745.1:n.*1489A=
ENST00000698473.1:n.3064A=
ENST00000698474.1:n.3064A=
ENST00000698475.1:n.3149A=
ENST00000698476.1:c.2524A= ENSP00000513746.1:p.Asn842=
ENST00000698477.1:c.2450A= ENSP00000513747.1:p.Lys817=
ENST00000698478.1:n.3064A=
ENST00000698479.1:c.2524A= ENSP00000513748.1:p.Asn842=
ENST00000698480.1:c.2445A= ENSP00000513749.1:p.Glu815=
ENST00000698481.1:c.2445A= ENSP00000513750.1:p.Glu815=
ENST00000698482.1:n.2814A=
ENST00000698483.1:n.2979A=
ENST00000698484.1:c.2524A= ENSP00000513751.1:p.Asn842=
ENST00000698485.1:c.2445A= ENSP00000513752.1:p.Glu815=
ENST00000698486.1:n.3064A=
ENST00000698487.1:c.2524A= ENSP00000513753.1:p.Asn842=
ENST00000698488.1:c.2268A= ENSP00000513754.1:p.Glu756=
ENST00000698489.1:n.6849A=
ENST00000698490.1:c.2524A= ENSP00000513755.1:p.Asn842=
ENST00000698492.1:c.*1239A= ENSP00000513756.1:n.*1239A=
ENST00000698493.1:n.2814A=
ENST00000698494.1:c.*504A= ENSP00000513757.1:n.*504A=
ENST00000358746.7:c.2524A= MANE Select ENSP00000351596.3:p.Asn842=
ENST00000649566.1:c.2524A= ENSP00000497948.1:p.Asn842=
ENST00000358746.6:c.2524A= ENSP00000351596.2:p.Asn842=
ENST00000506007.1:n.191A=
ENST00000507805.5:n.796A=
ENST00000508181.5:n.97A=
NM_014639.3:c.2524A= , LRG_173t1:c.2524A= NP_055454.1:p.Asn842=
XR_948312.1:n.2793A=
XR_001742370.2:n.2796A=
NM_014639.4:c.2524A= MANE Select NP_055454.1:p.Asn842=