Canonical Allele Identifier: CA2695223734
Gene: CHST6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.75479382_75479383dup , CM000678.2:g.75479382_75479383dup GRCh38
NC_000016.9:g.75513280_75513281dup , CM000678.1:g.75513280_75513281dup GRCh37
NC_000016.8:g.74070781_74070782dup NCBI36
NG_016442.1:g.20646_20647dup
NG_016442.2:g.21059_21060dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332272.9:c.446_447dup MANE Select ENSP00000328983.4:p.Lys150AlafsTer?
ENST00000390664.3:c.446_447dup ENSP00000375079.2:p.Lys150AlafsTer?
ENST00000649341.1:c.446_447dup ENSP00000497635.1:p.Lys150AlafsTer?
ENST00000649824.1:c.446_447dup ENSP00000496806.1:p.Lys150AlafsTer?
ENST00000332272.8:c.446_447dup ENSP00000328983.4:p.Lys150AlafsTer?
ENST00000390664.2:c.446_447dup ENSP00000375079.2:p.Lys150AlafsTer?
NM_021615.4:c.446_447dup NP_067628.1:p.Lys150AlafsTer?
XM_005255955.3:c.446_447dup XP_005256012.1:p.Lys150AlafsTer?
XM_011523085.1:c.446_447dup XP_011521387.1:p.Lys150AlafsTer?
NM_021615.5:c.446_447dup MANE Select NP_067628.1:p.Lys150AlafsTer?
XM_005255955.5:c.446_447dup XP_005256012.1:p.Lys150AlafsTer?
XM_011523085.3:c.446_447dup XP_011521387.1:p.Lys150AlafsTer?
NR_163480.1:n.733+2434_733+2435dup
NR_163481.1:n.577+2434_577+2435dup