Canonical Allele Identifier: CA351079806

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233672529G>C , CM000664.2:g.233672529G>C GRCh38
NC_000002.11:g.234581175G>C , CM000664.1:g.234581175G>C GRCh37
NC_000002.10:g.234245914G>C NCBI36
NG_002601.2:g.87786G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344644.10:c.855+35152G>C (UGT1A10) MANE Select ENSP00000343838.5:n.855+35152G>C
ENST00000373450.5:c.855+53967G>C (UGT1A8) MANE Select ENSP00000362549.4:n.855+53967G>C
ENST00000354728.5:c.595G>C (UGT1A9) MANE Select ENSP00000346768.4:p.Asp199His
ENST00000344644.9:c.855+35152G>C (UGT1A10) ENSP00000343838.5:n.855+35152G>C
ENST00000354728.4:c.595G>C (UGT1A9) ENSP00000346768.4:p.Asp199His
ENST00000373445.1:c.855+35152G>C (UGT1A10) ENSP00000362544.1:n.855+35152G>C
ENST00000373450.4:c.855+53967G>C (UGT1A8) ENSP00000362549.4:n.855+53967G>C
NM_019075.2:c.855+35152G>C (UGT1A10) NP_061948.1:n.855+35152G>C
NM_019076.4:c.855+53967G>C (UGT1A8) NP_061949.3:n.855+53967G>C
NM_021027.2:c.595G>C (UGT1A9) NP_066307.1:p.Asp199His
NM_021027.3:c.595G>C (UGT1A9) MANE Select NP_066307.1:p.Asp199His
NM_019075.4:c.855+35152G>C (UGT1A10) MANE Select NP_061948.1:n.855+35152G>C
NM_019076.5:c.855+53967G>C (UGT1A8) MANE Select NP_061949.3:n.855+53967G>C