Canonical Allele Identifier: CA2233371570

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479075_75479081delinsTGCGTAC , CM000678.2:g.75479075_75479081delinsTGCGTAC	GRCh38
NC_000016.9:g.75512973_75512979delinsTGCGTAC , CM000678.1:g.75512973_75512979delinsTGCGTAC	GRCh37
NC_000016.8:g.74070474_74070480delinsTGCGTAC	NCBI36
NG_016442.1:g.20948_20954delinsGTACGCA
NG_016442.2:g.21361_21367delinsGTACGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.748_754delinsGTACGCA MANE Select	ENSP00000328983.4:p.Val250=
ENST00000390664.3:c.748_754delinsGTACGCA	ENSP00000375079.2:p.Val250=
ENST00000649341.1:c.748_754delinsGTACGCA	ENSP00000497635.1:p.Val250=
ENST00000649824.1:c.748_754delinsGTACGCA	ENSP00000496806.1:p.Val250=
ENST00000332272.8:c.748_754delinsGTACGCA	ENSP00000328983.4:p.Val250=
ENST00000390664.2:c.748_754delinsGTACGCA	ENSP00000375079.2:p.Val250=
NM_021615.4:c.748_754delinsGTACGCA	NP_067628.1:p.Val250=
XM_005255955.3:c.748_754delinsGTACGCA	XP_005256012.1:p.Val250=
XM_011523085.1:c.748_754delinsGTACGCA	XP_011521387.1:p.Val250=
NM_021615.5:c.748_754delinsGTACGCA MANE Select	NP_067628.1:p.Val250=
XM_005255955.5:c.748_754delinsGTACGCA	XP_005256012.1:p.Val250=
XM_011523085.3:c.748_754delinsGTACGCA	XP_011521387.1:p.Val250=
NR_163480.1:n.733+2736_733+2742delinsGTACGCA
NR_163481.1:n.577+2736_577+2742delinsGTACGCA