Canonical Allele Identifier: CA351067226

Gene: UGT1A10 UGT1A8

Linked Data

• MyVariant Identifiers: chr2:g.234546004A>G (hg19) ; chr2:g.233637358A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233637358A>G , CM000664.2:g.233637358A>G	GRCh38
NC_000002.11:g.234546004A>G , CM000664.1:g.234546004A>G	GRCh37
NC_000002.10:g.234210743A>G	NCBI36
NG_002601.2:g.52615A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.836A>G (UGT1A10) MANE Select	ENSP00000343838.5:p.Gln279Arg
ENST00000373450.5:c.855+18796A>G (UGT1A8) MANE Select	ENSP00000362549.4:n.855+18796A>G
ENST00000344644.9:c.836A>G (UGT1A10)	ENSP00000343838.5:p.Gln279Arg
ENST00000373445.1:c.836A>G (UGT1A10)	ENSP00000362544.1:p.Gln279Arg
ENST00000373450.4:c.855+18796A>G (UGT1A8)	ENSP00000362549.4:n.855+18796A>G
NM_019075.2:c.836A>G (UGT1A10)	NP_061948.1:p.Gln279Arg
NM_019076.4:c.855+18796A>G (UGT1A8)	NP_061949.3:n.855+18796A>G
NM_019075.4:c.836A>G (UGT1A10) MANE Select	NP_061948.1:p.Gln279Arg
NM_019076.5:c.855+18796A>G (UGT1A8) MANE Select	NP_061949.3:n.855+18796A>G