Canonical Allele Identifier: CA67607274
Gene: UGT1A10 HGNC NCBI
UGT1A8 HGNC NCBI

Linked Data

dbSNP Id: rs6714486

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233671659T>A , CM000664.2:g.233671659T>A GRCh38
NC_000002.11:g.234580305T>A , CM000664.1:g.234580305T>A GRCh37
NC_000002.10:g.234245044T>A NCBI36
NG_002601.2:g.86916T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.10:c.855+34282T>A (UGT1A10) MANE Select ENSP00000343838.5:p.=
ENST00000373450.5:c.855+53097T>A (UGT1A8) MANE Select ENSP00000362549.4:p.=
ENST00000344644.9:c.855+34282T>A (UGT1A10) ENSP00000343838.5:p.=
ENST00000373445.1:c.855+34282T>A (UGT1A10) ENSP00000362544.1:p.=
ENST00000373450.4:c.855+53097T>A (UGT1A8) ENSP00000362549.4:p.=
NM_019075.2:c.855+34282T>A (UGT1A10) NP_061948.1:p.=
NM_019076.4:c.855+53097T>A (UGT1A8) NP_061949.3:p.=
NM_019075.4:c.855+34282T>A (UGT1A10) MANE Select NP_061948.1:p.=
NM_019076.5:c.855+53097T>A (UGT1A8) MANE Select NP_061949.3:p.=