Canonical Allele Identifier: CA2695223727

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479172_75479173insCAG , CM000678.2:g.75479172_75479173insCAG	GRCh38
NC_000016.9:g.75513070_75513071insCAG , CM000678.1:g.75513070_75513071insCAG	GRCh37
NC_000016.8:g.74070571_74070572insCAG	NCBI36
NG_016442.1:g.20856_20857insCTG
NG_016442.2:g.21269_21270insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.656_657insCTG MANE Select	ENSP00000328983.4:p.Ala219_Arg220insTrp
ENST00000390664.3:c.656_657insCTG	ENSP00000375079.2:p.Ala219_Arg220insTrp
ENST00000649341.1:c.656_657insCTG	ENSP00000497635.1:p.Ala219_Arg220insTrp
ENST00000649824.1:c.656_657insCTG	ENSP00000496806.1:p.Ala219_Arg220insTrp
ENST00000332272.8:c.656_657insCTG	ENSP00000328983.4:p.Ala219_Arg220insTrp
ENST00000390664.2:c.656_657insCTG	ENSP00000375079.2:p.Ala219_Arg220insTrp
NM_021615.4:c.656_657insCTG	NP_067628.1:p.Ala219_Arg220insTrp
XM_005255955.3:c.656_657insCTG	XP_005256012.1:p.Ala219_Arg220insTrp
XM_011523085.1:c.656_657insCTG	XP_011521387.1:p.Ala219_Arg220insTrp
NM_021615.5:c.656_657insCTG MANE Select	NP_067628.1:p.Ala219_Arg220insTrp
XM_005255955.5:c.656_657insCTG	XP_005256012.1:p.Ala219_Arg220insTrp
XM_011523085.3:c.656_657insCTG	XP_011521387.1:p.Ala219_Arg220insTrp
NR_163480.1:n.733+2644_733+2645insCTG
NR_163481.1:n.577+2644_577+2645insCTG