Canonical Allele Identifier: CA1335850934
Gene: UGT1A10 HGNC NCBI
UGT1A8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233671478T= , CM000664.2:g.233671478T= GRCh38
NC_000002.11:g.234580124T= , CM000664.1:g.234580124T= GRCh37
NC_000002.10:g.234244863T= NCBI36
NG_002601.2:g.86735T=

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.10:c.855+34101T= (UGT1A10) MANE Select ENSP00000343838.5:n.855+34101T=
ENST00000373450.5:c.855+52916T= (UGT1A8) MANE Select ENSP00000362549.4:n.855+52916T=
ENST00000344644.9:c.855+34101T= (UGT1A10) ENSP00000343838.5:n.855+34101T=
ENST00000373445.1:c.855+34101T= (UGT1A10) ENSP00000362544.1:n.855+34101T=
ENST00000373450.4:c.855+52916T= (UGT1A8) ENSP00000362549.4:n.855+52916T=
NM_019075.2:c.855+34101T= (UGT1A10) NP_061948.1:n.855+34101T=
NM_019076.4:c.855+52916T= (UGT1A8) NP_061949.3:n.855+52916T=
NM_019075.4:c.855+34101T= (UGT1A10) MANE Select NP_061948.1:n.855+34101T=
NM_019076.5:c.855+52916T= (UGT1A8) MANE Select NP_061949.3:n.855+52916T=
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