Canonical Allele Identifier: CA2634344941
Gene: CHST6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.75479274dup , CM000678.2:g.75479274dup GRCh38
NC_000016.9:g.75513172dup , CM000678.1:g.75513172dup GRCh37
NC_000016.8:g.74070673dup NCBI36
NG_016442.1:g.20757dup
NG_016442.2:g.21170dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332272.9:c.557dup MANE Select ENSP00000328983.4:p.Leu187AlafsTer?
ENST00000390664.3:c.557dup ENSP00000375079.2:p.Leu187AlafsTer?
ENST00000649341.1:c.557dup ENSP00000497635.1:p.Leu187AlafsTer?
ENST00000649824.1:c.557dup ENSP00000496806.1:p.Leu187AlafsTer?
ENST00000332272.8:c.557dup ENSP00000328983.4:p.Leu187AlafsTer?
ENST00000390664.2:c.557dup ENSP00000375079.2:p.Leu187AlafsTer?
NM_021615.4:c.557dup NP_067628.1:p.Leu187AlafsTer?
XM_005255955.3:c.557dup XP_005256012.1:p.Leu187AlafsTer?
XM_011523085.1:c.557dup XP_011521387.1:p.Leu187AlafsTer?
NM_021615.5:c.557dup MANE Select NP_067628.1:p.Leu187AlafsTer?
XM_005255955.5:c.557dup XP_005256012.1:p.Leu187AlafsTer?
XM_011523085.3:c.557dup XP_011521387.1:p.Leu187AlafsTer?
NR_163480.1:n.733+2545dup
NR_163481.1:n.577+2545dup