Canonical Allele Identifier: CA2663711745

Gene: UGT1A10 UGT1A8

Linked Data

• dbSNP Id: rs2125459929
• gnomAD v4: 2-233637517-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233637519del , CM000664.2:g.233637519del	GRCh38
NC_000002.11:g.234546165del , CM000664.1:g.234546165del	GRCh37
NC_000002.10:g.234210904del	NCBI36
NG_002601.2:g.52776del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.855+142del (UGT1A10) MANE Select	ENSP00000343838.5:n.855+142del
ENST00000373450.5:c.855+18957del (UGT1A8) MANE Select	ENSP00000362549.4:n.855+18957del
ENST00000344644.9:c.855+142del (UGT1A10)	ENSP00000343838.5:n.855+142del
ENST00000373445.1:c.855+142del (UGT1A10)	ENSP00000362544.1:n.855+142del
ENST00000373450.4:c.855+18957del (UGT1A8)	ENSP00000362549.4:n.855+18957del
NM_019075.2:c.855+142del (UGT1A10)	NP_061948.1:n.855+142del
NM_019076.4:c.855+18957del (UGT1A8)	NP_061949.3:n.855+18957del
NM_019075.4:c.855+142del (UGT1A10) MANE Select	NP_061948.1:n.855+142del
NM_019076.5:c.855+18957del (UGT1A8) MANE Select	NP_061949.3:n.855+18957del