Canonical Allele Identifier: CA2754690889

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233672725_233672726insAAACA , CM000664.2:g.233672725_233672726insAAACA GRCh38
NC_000002.11:g.234581371_234581372insAAACA , CM000664.1:g.234581371_234581372insAAACA GRCh37
NC_000002.10:g.234246110_234246111insAAACA NCBI36
NG_002601.2:g.87982_87983insAAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000344644.10:c.855+35348_855+35349insAAACA (UGT1A10) MANE Select ENSP00000343838.5:n.855+35348_855+35349insAAACA
ENST00000373450.5:c.855+54163_855+54164insAAACA (UGT1A8) MANE Select ENSP00000362549.4:n.855+54163_855+54164insAAACA
ENST00000354728.5:c.791_792insAAACA (UGT1A9) MANE Select ENSP00000346768.4:p.Val265AsnfsTer3
ENST00000344644.9:c.855+35348_855+35349insAAACA (UGT1A10) ENSP00000343838.5:n.855+35348_855+35349insAAACA
ENST00000354728.4:c.791_792insAAACA (UGT1A9) ENSP00000346768.4:p.Val265AsnfsTer3
ENST00000373445.1:c.855+35348_855+35349insAAACA (UGT1A10) ENSP00000362544.1:n.855+35348_855+35349insAAACA
ENST00000373450.4:c.855+54163_855+54164insAAACA (UGT1A8) ENSP00000362549.4:n.855+54163_855+54164insAAACA
NM_019075.2:c.855+35348_855+35349insAAACA (UGT1A10) NP_061948.1:n.855+35348_855+35349insAAACA
NM_019076.4:c.855+54163_855+54164insAAACA (UGT1A8) NP_061949.3:n.855+54163_855+54164insAAACA
NM_021027.2:c.791_792insAAACA (UGT1A9) NP_066307.1:p.Val265AsnfsTer3
NM_021027.3:c.791_792insAAACA (UGT1A9) MANE Select NP_066307.1:p.Val265AsnfsTer3
NM_019075.4:c.855+35348_855+35349insAAACA (UGT1A10) MANE Select NP_061948.1:n.855+35348_855+35349insAAACA
NM_019076.5:c.855+54163_855+54164insAAACA (UGT1A8) MANE Select NP_061949.3:n.855+54163_855+54164insAAACA