Canonical Allele Identifier: CA1335854475
Gene: UGT1A10 HGNC NCBI
UGT1A8 HGNC NCBI
UGT1A9 HGNC NCBI

Linked Data

dbSNP Id: rs2074325076
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233675502C>G , CM000664.2:g.233675502C>G GRCh38
NC_000002.11:g.234584148C>G , CM000664.1:g.234584148C>G GRCh37
NC_000002.10:g.234248887C>G NCBI36
NG_002601.2:g.90759C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.10:c.855+38125C>G (UGT1A10) MANE Select ENSP00000343838.5:n.855+38125C>G
ENST00000373450.5:c.855+56940C>G (UGT1A8) MANE Select ENSP00000362549.4:n.855+56940C>G
ENST00000354728.5:c.855+2713C>G (UGT1A9) MANE Select ENSP00000346768.4:n.855+2713C>G
ENST00000344644.9:c.855+38125C>G (UGT1A10) ENSP00000343838.5:n.855+38125C>G
ENST00000354728.4:c.855+2713C>G (UGT1A9) ENSP00000346768.4:n.855+2713C>G
ENST00000373445.1:c.855+38125C>G (UGT1A10) ENSP00000362544.1:n.855+38125C>G
ENST00000373450.4:c.855+56940C>G (UGT1A8) ENSP00000362549.4:n.855+56940C>G
NM_019075.2:c.855+38125C>G (UGT1A10) NP_061948.1:n.855+38125C>G
NM_019076.4:c.855+56940C>G (UGT1A8) NP_061949.3:n.855+56940C>G
NM_021027.2:c.855+2713C>G (UGT1A9) NP_066307.1:n.855+2713C>G
NM_021027.3:c.855+2713C>G (UGT1A9) MANE Select NP_066307.1:n.855+2713C>G
NM_019075.4:c.855+38125C>G (UGT1A10) MANE Select NP_061948.1:n.855+38125C>G
NM_019076.5:c.855+56940C>G (UGT1A8) MANE Select NP_061949.3:n.855+56940C>G
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