Canonical Allele Identifier: CA645590702
Gene: CHST6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.75479338dup , CM000678.2:g.75479338dup GRCh38
NC_000016.9:g.75513236dup , CM000678.1:g.75513236dup GRCh37
NC_000016.8:g.74070737dup NCBI36
NG_016442.1:g.20692dup
NG_016442.2:g.21105dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332272.9:c.492dup MANE Select ENSP00000328983.4:p.Cys165LeufsTer?
ENST00000390664.3:c.492dup ENSP00000375079.2:p.Cys165LeufsTer?
ENST00000649341.1:c.492dup ENSP00000497635.1:p.Cys165LeufsTer?
ENST00000649824.1:c.492dup ENSP00000496806.1:p.Cys165LeufsTer?
ENST00000332272.8:c.492dup ENSP00000328983.4:p.Cys165LeufsTer?
ENST00000390664.2:c.492dup ENSP00000375079.2:p.Cys165LeufsTer?
NM_021615.4:c.492dup NP_067628.1:p.Cys165LeufsTer?
XM_005255955.3:c.492dup XP_005256012.1:p.Cys165LeufsTer?
XM_011523085.1:c.492dup XP_011521387.1:p.Cys165LeufsTer?
NM_021615.5:c.492dup MANE Select NP_067628.1:p.Cys165LeufsTer?
XM_005255955.5:c.492dup XP_005256012.1:p.Cys165LeufsTer?
XM_011523085.3:c.492dup XP_011521387.1:p.Cys165LeufsTer?
NR_163480.1:n.733+2480dup
NR_163481.1:n.577+2480dup