Canonical Allele Identifier: CA2634344409
Gene: CHST6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.75479053_75479066del , CM000678.2:g.75479053_75479066del GRCh38
NC_000016.9:g.75512951_75512964del , CM000678.1:g.75512951_75512964del GRCh37
NC_000016.8:g.74070452_74070465del NCBI36
NG_016442.1:g.20971_20984del
NG_016442.2:g.21384_21397del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332272.9:c.771_784del MANE Select ENSP00000328983.4:p.Lys259SerfsTer?
ENST00000390664.3:c.771_784del ENSP00000375079.2:p.Lys259SerfsTer?
ENST00000649341.1:c.771_784del ENSP00000497635.1:p.Lys259SerfsTer?
ENST00000649824.1:c.771_784del ENSP00000496806.1:p.Lys259SerfsTer?
ENST00000332272.8:c.771_784del ENSP00000328983.4:p.Lys259SerfsTer?
ENST00000390664.2:c.771_784del ENSP00000375079.2:p.Lys259SerfsTer?
NM_021615.4:c.771_784del NP_067628.1:p.Lys259SerfsTer?
XM_005255955.3:c.771_784del XP_005256012.1:p.Lys259SerfsTer?
XM_011523085.1:c.771_784del XP_011521387.1:p.Lys259SerfsTer?
NM_021615.5:c.771_784del MANE Select NP_067628.1:p.Lys259SerfsTer?
XM_005255955.5:c.771_784del XP_005256012.1:p.Lys259SerfsTer?
XM_011523085.3:c.771_784del XP_011521387.1:p.Lys259SerfsTer?
NR_163480.1:n.733+2759_733+2772del
NR_163481.1:n.577+2759_577+2772del