Canonical Allele Identifier: CA2233371056

Gene: CHST6

Linked Data

• dbSNP Id: rs2080101623

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75478999_75479037del , CM000678.2:g.75478999_75479037del	GRCh38
NC_000016.9:g.75512897_75512935del , CM000678.1:g.75512897_75512935del	GRCh37
NC_000016.8:g.74070398_74070436del	NCBI36
NG_016442.1:g.20995_21033del
NG_016442.2:g.21408_21446del

Transcript Alleles

HGVS	Amino-acid change
ENST00000332272.9:c.795_833del MANE Select	ENSP00000328983.4:p.Gly266_Arg278del
ENST00000390664.3:c.795_833del	ENSP00000375079.2:p.Gly266_Arg278del
ENST00000649341.1:c.795_833del	ENSP00000497635.1:p.Gly266_Arg278del
ENST00000649824.1:c.795_833del	ENSP00000496806.1:p.Gly266_Arg278del
ENST00000332272.8:c.795_833del	ENSP00000328983.4:p.Gly266_Arg278del
ENST00000390664.2:c.795_833del	ENSP00000375079.2:p.Gly266_Arg278del
NM_021615.4:c.795_833del	NP_067628.1:p.Gly266_Arg278del
XM_005255955.3:c.795_833del	XP_005256012.1:p.Gly266_Arg278del
XM_011523085.1:c.795_833del	XP_011521387.1:p.Gly266_Arg278del
NM_021615.5:c.795_833del MANE Select	NP_067628.1:p.Gly266_Arg278del
XM_005255955.5:c.795_833del	XP_005256012.1:p.Gly266_Arg278del
XM_011523085.3:c.795_833del	XP_011521387.1:p.Gly266_Arg278del
NR_163480.1:n.733+2783_733+2821del
NR_163481.1:n.577+2783_577+2821del