Canonical Allele Identifier: CA1043552075

Linked Data

dbSNP Id: rs2074327303

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233675548_233675549del , CM000664.2:g.233675548_233675549del GRCh38
NC_000002.11:g.234584194_234584195del , CM000664.1:g.234584194_234584195del GRCh37
NC_000002.10:g.234248933_234248934del NCBI36
NG_002601.2:g.90805_90806del

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.10:c.855+38171_855+38172del (UGT1A10) MANE Select ENSP00000343838.5:n.855+38171_855+38172del
ENST00000373450.5:c.855+56986_855+56987del (UGT1A8) MANE Select ENSP00000362549.4:n.855+56986_855+56987del
ENST00000354728.5:c.855+2759_855+2760del (UGT1A9) MANE Select ENSP00000346768.4:n.855+2759_855+2760del
ENST00000344644.9:c.855+38171_855+38172del (UGT1A10) ENSP00000343838.5:n.855+38171_855+38172del
ENST00000354728.4:c.855+2759_855+2760del (UGT1A9) ENSP00000346768.4:n.855+2759_855+2760del
ENST00000373445.1:c.855+38171_855+38172del (UGT1A10) ENSP00000362544.1:n.855+38171_855+38172del
ENST00000373450.4:c.855+56986_855+56987del (UGT1A8) ENSP00000362549.4:n.855+56986_855+56987del
NM_019075.2:c.855+38171_855+38172del (UGT1A10) NP_061948.1:n.855+38171_855+38172del
NM_019076.4:c.855+56986_855+56987del (UGT1A8) NP_061949.3:n.855+56986_855+56987del
NM_021027.2:c.855+2759_855+2760del (UGT1A9) NP_066307.1:n.855+2759_855+2760del
NM_021027.3:c.855+2759_855+2760del (UGT1A9) MANE Select NP_066307.1:n.855+2759_855+2760del
NM_019075.4:c.855+38171_855+38172del (UGT1A10) MANE Select NP_061948.1:n.855+38171_855+38172del
NM_019076.5:c.855+56986_855+56987del (UGT1A8) MANE Select NP_061949.3:n.855+56986_855+56987del