Canonical Allele Identifier: CA2233373116

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479382_75479384delinsGCA , CM000678.2:g.75479382_75479384delinsGCA	GRCh38
NC_000016.9:g.75513280_75513282delinsGCA , CM000678.1:g.75513280_75513282delinsGCA	GRCh37
NC_000016.8:g.74070781_74070783delinsGCA	NCBI36
NG_016442.1:g.20645_20647delinsTGC
NG_016442.2:g.21058_21060delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.445_447delinsTGC MANE Select	ENSP00000328983.4:p.Cys149=
ENST00000390664.3:c.445_447delinsTGC	ENSP00000375079.2:p.Cys149=
ENST00000649341.1:c.445_447delinsTGC	ENSP00000497635.1:p.Cys149=
ENST00000649824.1:c.445_447delinsTGC	ENSP00000496806.1:p.Cys149=
ENST00000332272.8:c.445_447delinsTGC	ENSP00000328983.4:p.Cys149=
ENST00000390664.2:c.445_447delinsTGC	ENSP00000375079.2:p.Cys149=
NM_021615.4:c.445_447delinsTGC	NP_067628.1:p.Cys149=
XM_005255955.3:c.445_447delinsTGC	XP_005256012.1:p.Cys149=
XM_011523085.1:c.445_447delinsTGC	XP_011521387.1:p.Cys149=
NM_021615.5:c.445_447delinsTGC MANE Select	NP_067628.1:p.Cys149=
XM_005255955.5:c.445_447delinsTGC	XP_005256012.1:p.Cys149=
XM_011523085.3:c.445_447delinsTGC	XP_011521387.1:p.Cys149=
NR_163480.1:n.733+2433_733+2435delinsTGC
NR_163481.1:n.577+2433_577+2435delinsTGC