Canonical Allele Identifier: CA2695223730

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479242_75479244dup , CM000678.2:g.75479242_75479244dup	GRCh38
NC_000016.9:g.75513140_75513142dup , CM000678.1:g.75513140_75513142dup	GRCh37
NC_000016.8:g.74070641_74070643dup	NCBI36
NG_016442.1:g.20785_20787dup
NG_016442.2:g.21198_21200dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.585_587dup MANE Select	ENSP00000328983.4:p.Arg196_Ile197insArg
ENST00000390664.3:c.585_587dup	ENSP00000375079.2:p.Arg196_Ile197insArg
ENST00000649341.1:c.585_587dup	ENSP00000497635.1:p.Arg196_Ile197insArg
ENST00000649824.1:c.585_587dup	ENSP00000496806.1:p.Arg196_Ile197insArg
ENST00000332272.8:c.585_587dup	ENSP00000328983.4:p.Arg196_Ile197insArg
ENST00000390664.2:c.585_587dup	ENSP00000375079.2:p.Arg196_Ile197insArg
NM_021615.4:c.585_587dup	NP_067628.1:p.Arg196_Ile197insArg
XM_005255955.3:c.585_587dup	XP_005256012.1:p.Arg196_Ile197insArg
XM_011523085.1:c.585_587dup	XP_011521387.1:p.Arg196_Ile197insArg
NM_021615.5:c.585_587dup MANE Select	NP_067628.1:p.Arg196_Ile197insArg
XM_005255955.5:c.585_587dup	XP_005256012.1:p.Arg196_Ile197insArg
XM_011523085.3:c.585_587dup	XP_011521387.1:p.Arg196_Ile197insArg
NR_163480.1:n.733+2573_733+2575dup
NR_163481.1:n.577+2573_577+2575dup