Canonical Allele Identifier: CA1335835099

Gene: UGT1A10 UGT1A8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233637367C= , CM000664.2:g.233637367C=	GRCh38
NC_000002.11:g.234546013C= , CM000664.1:g.234546013C=	GRCh37
NC_000002.10:g.234210752C=	NCBI36
NG_002601.2:g.52624C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.845C= (UGT1A10) MANE Select	ENSP00000343838.5:p.Pro282=
ENST00000373450.5:c.855+18805C= (UGT1A8) MANE Select	ENSP00000362549.4:n.855+18805C=
ENST00000344644.9:c.845C= (UGT1A10)	ENSP00000343838.5:p.Pro282=
ENST00000373445.1:c.845C= (UGT1A10)	ENSP00000362544.1:p.Pro282=
ENST00000373450.4:c.855+18805C= (UGT1A8)	ENSP00000362549.4:n.855+18805C=
NM_019075.2:c.845C= (UGT1A10)	NP_061948.1:p.Pro282=
NM_019076.4:c.855+18805C= (UGT1A8)	NP_061949.3:n.855+18805C=
NM_019075.4:c.845C= (UGT1A10) MANE Select	NP_061948.1:p.Pro282=
NM_019076.5:c.855+18805C= (UGT1A8) MANE Select	NP_061949.3:n.855+18805C=