Canonical Allele Identifier: CA2838234477

Gene: CHST11

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.104733614C>A , CM000674.2:g.104733614C>A	GRCh38
NC_000012.11:g.105127392C>A , CM000674.1:g.105127392C>A	GRCh37
NC_000012.10:g.103651522C>A	NCBI36
NG_029810.1:g.281701C>A
NG_029810.2:g.281701C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303694.6:c.205-23335C>A MANE Select	ENSP00000305725.5:n.205-23335C>A
ENST00000303694.5:c.205-23335C>A	ENSP00000305725.5:n.205-23335C>A
ENST00000549016.1:c.85-23335C>A	ENSP00000449095.1:n.85-23335C>A
ENST00000549260.5:c.190-23335C>A	ENSP00000450004.1:n.190-23335C>A
NM_001173982.1:c.190-23335C>A	NP_001167453.1:n.190-23335C>A
NM_018413.5:c.205-23335C>A	NP_060883.1:n.205-23335C>A
XM_017019369.1:c.210-4003C>A	XP_016874858.1:n.210-4003C>A
NM_018413.6:c.205-23335C>A MANE Select	NP_060883.1:n.205-23335C>A
NM_001173982.2:c.190-23335C>A	NP_001167453.1:n.190-23335C>A