Canonical Allele Identifier: CA2060248089

Gene: CHST11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.104623386C= , CM000674.2:g.104623386C=	GRCh38
NC_000012.11:g.105017164C= , CM000674.1:g.105017164C=	GRCh37
NC_000012.10:g.103541294C=	NCBI36
NG_029810.1:g.171473C=
NG_029810.2:g.171473C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303694.6:c.204+21395C= MANE Select	ENSP00000305725.5:n.204+21395C=
ENST00000303694.5:c.204+21395C=	ENSP00000305725.5:n.204+21395C=
ENST00000549016.1:c.84+21395C=	ENSP00000449095.1:n.84+21395C=
ENST00000549260.5:c.189+21395C=	ENSP00000450004.1:n.189+21395C=
NM_001173982.1:c.189+21395C=	NP_001167453.1:n.189+21395C=
NM_018413.5:c.204+21395C=	NP_060883.1:n.204+21395C=
XM_017019369.1:c.209+21395C=	XP_016874858.1:n.209+21395C=
NM_018413.6:c.204+21395C= MANE Select	NP_060883.1:n.204+21395C=
NM_001173982.2:c.189+21395C=	NP_001167453.1:n.189+21395C=