Canonical Allele Identifier: CA2233371714

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479098_75479107delinsTCGCGCACCA , CM000678.2:g.75479098_75479107delinsTCGCGCACCA	GRCh38
NC_000016.9:g.75512996_75513005delinsTCGCGCACCA , CM000678.1:g.75512996_75513005delinsTCGCGCACCA	GRCh37
NC_000016.8:g.74070497_74070506delinsTCGCGCACCA	NCBI36
NG_016442.1:g.20922_20931delinsTGGTGCGCGA
NG_016442.2:g.21335_21344delinsTGGTGCGCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.722_731delinsTGGTGCGCGA MANE Select	ENSP00000328983.4:p.Val241=
ENST00000390664.3:c.722_731delinsTGGTGCGCGA	ENSP00000375079.2:p.Val241=
ENST00000649341.1:c.722_731delinsTGGTGCGCGA	ENSP00000497635.1:p.Val241=
ENST00000649824.1:c.722_731delinsTGGTGCGCGA	ENSP00000496806.1:p.Val241=
ENST00000332272.8:c.722_731delinsTGGTGCGCGA	ENSP00000328983.4:p.Val241=
ENST00000390664.2:c.722_731delinsTGGTGCGCGA	ENSP00000375079.2:p.Val241=
NM_021615.4:c.722_731delinsTGGTGCGCGA	NP_067628.1:p.Val241=
XM_005255955.3:c.722_731delinsTGGTGCGCGA	XP_005256012.1:p.Val241=
XM_011523085.1:c.722_731delinsTGGTGCGCGA	XP_011521387.1:p.Val241=
NM_021615.5:c.722_731delinsTGGTGCGCGA MANE Select	NP_067628.1:p.Val241=
XM_005255955.5:c.722_731delinsTGGTGCGCGA	XP_005256012.1:p.Val241=
XM_011523085.3:c.722_731delinsTGGTGCGCGA	XP_011521387.1:p.Val241=
NR_163480.1:n.733+2710_733+2719delinsTGGTGCGCGA
NR_163481.1:n.577+2710_577+2719delinsTGGTGCGCGA