Canonical Allele Identifier: CA1335850967
Gene: UGT1A10 HGNC NCBI
UGT1A8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233671557G= , CM000664.2:g.233671557G= GRCh38
NC_000002.11:g.234580203G= , CM000664.1:g.234580203G= GRCh37
NC_000002.10:g.234244942G= NCBI36
NG_002601.2:g.86814G=

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.10:c.855+34180G= (UGT1A10) MANE Select ENSP00000343838.5:n.855+34180G=
ENST00000373450.5:c.855+52995G= (UGT1A8) MANE Select ENSP00000362549.4:n.855+52995G=
ENST00000344644.9:c.855+34180G= (UGT1A10) ENSP00000343838.5:n.855+34180G=
ENST00000373445.1:c.855+34180G= (UGT1A10) ENSP00000362544.1:n.855+34180G=
ENST00000373450.4:c.855+52995G= (UGT1A8) ENSP00000362549.4:n.855+52995G=
NM_019075.2:c.855+34180G= (UGT1A10) NP_061948.1:n.855+34180G=
NM_019076.4:c.855+52995G= (UGT1A8) NP_061949.3:n.855+52995G=
NM_019075.4:c.855+34180G= (UGT1A10) MANE Select NP_061948.1:n.855+34180G=
NM_019076.5:c.855+52995G= (UGT1A8) MANE Select NP_061949.3:n.855+52995G=
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