Canonical Allele Identifier: CA2695223726

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479146_75479147delinsTC , CM000678.2:g.75479146_75479147delinsTC	GRCh38
NC_000016.9:g.75513044_75513045delinsTC , CM000678.1:g.75513044_75513045delinsTC	GRCh37
NC_000016.8:g.74070545_74070546delinsTC	NCBI36
NG_016442.1:g.20882_20883delinsGA
NG_016442.2:g.21295_21296delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.682_683delinsGA MANE Select	ENSP00000328983.4:p.Thr228Asp
ENST00000390664.3:c.682_683delinsGA	ENSP00000375079.2:p.Thr228Asp
ENST00000649341.1:c.682_683delinsGA	ENSP00000497635.1:p.Thr228Asp
ENST00000649824.1:c.682_683delinsGA	ENSP00000496806.1:p.Thr228Asp
ENST00000332272.8:c.682_683delinsGA	ENSP00000328983.4:p.Thr228Asp
ENST00000390664.2:c.682_683delinsGA	ENSP00000375079.2:p.Thr228Asp
NM_021615.4:c.682_683delinsGA	NP_067628.1:p.Thr228Asp
XM_005255955.3:c.682_683delinsGA	XP_005256012.1:p.Thr228Asp
XM_011523085.1:c.682_683delinsGA	XP_011521387.1:p.Thr228Asp
NM_021615.5:c.682_683delinsGA MANE Select	NP_067628.1:p.Thr228Asp
XM_005255955.5:c.682_683delinsGA	XP_005256012.1:p.Thr228Asp
XM_011523085.3:c.682_683delinsGA	XP_011521387.1:p.Thr228Asp
NR_163480.1:n.733+2670_733+2671delinsGA
NR_163481.1:n.577+2670_577+2671delinsGA