Canonical Allele Identifier: CA2634344832
Gene: CHST6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.75479245_75479246insCCGTA , CM000678.2:g.75479245_75479246insCCGTA GRCh38
NC_000016.9:g.75513143_75513144insCCGTA , CM000678.1:g.75513143_75513144insCCGTA GRCh37
NC_000016.8:g.74070644_74070645insCCGTA NCBI36
NG_016442.1:g.20787_20788insGTACG
NG_016442.2:g.21200_21201insGTACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000332272.9:c.587_588insGTACG MANE Select ENSP00000328983.4:p.Ile197TyrfsTer?
ENST00000390664.3:c.587_588insGTACG ENSP00000375079.2:p.Ile197TyrfsTer?
ENST00000649341.1:c.587_588insGTACG ENSP00000497635.1:p.Ile197TyrfsTer?
ENST00000649824.1:c.587_588insGTACG ENSP00000496806.1:p.Ile197TyrfsTer?
ENST00000332272.8:c.587_588insGTACG ENSP00000328983.4:p.Ile197TyrfsTer?
ENST00000390664.2:c.587_588insGTACG ENSP00000375079.2:p.Ile197TyrfsTer?
NM_021615.4:c.587_588insGTACG NP_067628.1:p.Ile197TyrfsTer?
XM_005255955.3:c.587_588insGTACG XP_005256012.1:p.Ile197TyrfsTer?
XM_011523085.1:c.587_588insGTACG XP_011521387.1:p.Ile197TyrfsTer?
NM_021615.5:c.587_588insGTACG MANE Select NP_067628.1:p.Ile197TyrfsTer?
XM_005255955.5:c.587_588insGTACG XP_005256012.1:p.Ile197TyrfsTer?
XM_011523085.3:c.587_588insGTACG XP_011521387.1:p.Ile197TyrfsTer?
NR_163480.1:n.733+2575_733+2576insGTACG
NR_163481.1:n.577+2575_577+2576insGTACG