Canonical Allele Identifier: CA2233372170

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479164T= , CM000678.2:g.75479164T=	GRCh38
NC_000016.9:g.75513062T= , CM000678.1:g.75513062T=	GRCh37
NC_000016.8:g.74070563T=	NCBI36
NG_016442.1:g.20865A=
NG_016442.2:g.21278A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.665A= MANE Select	ENSP00000328983.4:p.Asn222=
ENST00000390664.3:c.665A=	ENSP00000375079.2:p.Asn222=
ENST00000649341.1:c.665A=	ENSP00000497635.1:p.Asn222=
ENST00000649824.1:c.665A=	ENSP00000496806.1:p.Asn222=
ENST00000332272.8:c.665A=	ENSP00000328983.4:p.Asn222=
ENST00000390664.2:c.665A=	ENSP00000375079.2:p.Asn222=
NM_021615.4:c.665A=	NP_067628.1:p.Asn222=
XM_005255955.3:c.665A=	XP_005256012.1:p.Asn222=
XM_011523085.1:c.665A=	XP_011521387.1:p.Asn222=
NM_021615.5:c.665A= MANE Select	NP_067628.1:p.Asn222=
XM_005255955.5:c.665A=	XP_005256012.1:p.Asn222=
XM_011523085.3:c.665A=	XP_011521387.1:p.Asn222=
NR_163480.1:n.733+2653A=
NR_163481.1:n.577+2653A=