Canonical Allele Identifier: CA1335835114
Gene: UGT1A10 HGNC NCBI
UGT1A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233637383_233637386delinsTCAC , CM000664.2:g.233637383_233637386delinsTCAC GRCh38
NC_000002.11:g.234546029_234546032delinsTCAC , CM000664.1:g.234546029_234546032delinsTCAC GRCh37
NC_000002.10:g.234210768_234210771delinsTCAC NCBI36
NG_002601.2:g.52640_52643delinsTCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000344644.10:c.855+6_855+9delinsTCAC (UGT1A10) MANE Select ENSP00000343838.5:n.855+6_855+9delinsTCAC
ENST00000373450.5:c.855+18821_855+18824delinsTCAC (UGT1A8) MANE Select ENSP00000362549.4:n.855+18821_855+18824delinsTCAC
ENST00000344644.9:c.855+6_855+9delinsTCAC (UGT1A10) ENSP00000343838.5:n.855+6_855+9delinsTCAC
ENST00000373445.1:c.855+6_855+9delinsTCAC (UGT1A10) ENSP00000362544.1:n.855+6_855+9delinsTCAC
ENST00000373450.4:c.855+18821_855+18824delinsTCAC (UGT1A8) ENSP00000362549.4:n.855+18821_855+18824delinsTCAC
NM_019075.2:c.855+6_855+9delinsTCAC (UGT1A10) NP_061948.1:n.855+6_855+9delinsTCAC
NM_019076.4:c.855+18821_855+18824delinsTCAC (UGT1A8) NP_061949.3:n.855+18821_855+18824delinsTCAC
NM_019075.4:c.855+6_855+9delinsTCAC (UGT1A10) MANE Select NP_061948.1:n.855+6_855+9delinsTCAC
NM_019076.5:c.855+18821_855+18824delinsTCAC (UGT1A8) MANE Select NP_061949.3:n.855+18821_855+18824delinsTCAC