Canonical Allele Identifier: CA2233373063

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479364_75479366delinsCCG , CM000678.2:g.75479364_75479366delinsCCG	GRCh38
NC_000016.9:g.75513262_75513264delinsCCG , CM000678.1:g.75513262_75513264delinsCCG	GRCh37
NC_000016.8:g.74070763_74070765delinsCCG	NCBI36
NG_016442.1:g.20663_20665delinsCGG
NG_016442.2:g.21076_21078delinsCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.463_465delinsCGG MANE Select	ENSP00000328983.4:p.Arg155=
ENST00000390664.3:c.463_465delinsCGG	ENSP00000375079.2:p.Arg155=
ENST00000649341.1:c.463_465delinsCGG	ENSP00000497635.1:p.Arg155=
ENST00000649824.1:c.463_465delinsCGG	ENSP00000496806.1:p.Arg155=
ENST00000332272.8:c.463_465delinsCGG	ENSP00000328983.4:p.Arg155=
ENST00000390664.2:c.463_465delinsCGG	ENSP00000375079.2:p.Arg155=
NM_021615.4:c.463_465delinsCGG	NP_067628.1:p.Arg155=
XM_005255955.3:c.463_465delinsCGG	XP_005256012.1:p.Arg155=
XM_011523085.1:c.463_465delinsCGG	XP_011521387.1:p.Arg155=
NM_021615.5:c.463_465delinsCGG MANE Select	NP_067628.1:p.Arg155=
XM_005255955.5:c.463_465delinsCGG	XP_005256012.1:p.Arg155=
XM_011523085.3:c.463_465delinsCGG	XP_011521387.1:p.Arg155=
NR_163480.1:n.733+2451_733+2453delinsCGG
NR_163481.1:n.577+2451_577+2453delinsCGG