Canonical Allele Identifier: CA2233372000

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479136_75479138delinsCGT , CM000678.2:g.75479136_75479138delinsCGT	GRCh38
NC_000016.9:g.75513034_75513036delinsCGT , CM000678.1:g.75513034_75513036delinsCGT	GRCh37
NC_000016.8:g.74070535_74070537delinsCGT	NCBI36
NG_016442.1:g.20891_20893delinsACG
NG_016442.2:g.21304_21306delinsACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.691_693delinsACG MANE Select	ENSP00000328983.4:p.Thr231=
ENST00000390664.3:c.691_693delinsACG	ENSP00000375079.2:p.Thr231=
ENST00000649341.1:c.691_693delinsACG	ENSP00000497635.1:p.Thr231=
ENST00000649824.1:c.691_693delinsACG	ENSP00000496806.1:p.Thr231=
ENST00000332272.8:c.691_693delinsACG	ENSP00000328983.4:p.Thr231=
ENST00000390664.2:c.691_693delinsACG	ENSP00000375079.2:p.Thr231=
NM_021615.4:c.691_693delinsACG	NP_067628.1:p.Thr231=
XM_005255955.3:c.691_693delinsACG	XP_005256012.1:p.Thr231=
XM_011523085.1:c.691_693delinsACG	XP_011521387.1:p.Thr231=
NM_021615.5:c.691_693delinsACG MANE Select	NP_067628.1:p.Thr231=
XM_005255955.5:c.691_693delinsACG	XP_005256012.1:p.Thr231=
XM_011523085.3:c.691_693delinsACG	XP_011521387.1:p.Thr231=
NR_163480.1:n.733+2679_733+2681delinsACG
NR_163481.1:n.577+2679_577+2681delinsACG