Canonical Allele Identifier: CA351093108

Gene: UGT1A10 UGT1A7 UGT1A8 UGT1A6 UGT1A9

Linked Data

• dbSNP Id: rs6759892
• gnomAD v3: 2-233693023-T-A
• gnomAD v4: 2-233693023-T-A
• MyVariant Identifiers: chr2:g.234601669T>A (hg19) ; chr2:g.233693023T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233693023T>A , CM000664.2:g.233693023T>A	GRCh38
NC_000002.11:g.234601669T>A , CM000664.1:g.234601669T>A	GRCh37
NC_000002.10:g.234266408T>A	NCBI36
NG_002601.2:g.108280T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.855+55646T>A (UGT1A10) MANE Select	ENSP00000343838.5:n.855+55646T>A
ENST00000373426.4:c.855+10231T>A (UGT1A7) MANE Select	ENSP00000362525.3:n.855+10231T>A
ENST00000373450.5:c.856-74011T>A (UGT1A8) MANE Select	ENSP00000362549.4:n.856-74011T>A
ENST00000305139.11:c.19T>A (UGT1A6) MANE Select	ENSP00000303174.6:p.Ser7Thr
ENST00000354728.5:c.855+20234T>A (UGT1A9) MANE Select	ENSP00000346768.4:n.855+20234T>A
ENST00000305139.10:c.19T>A (UGT1A6)	ENSP00000303174.6:p.Ser7Thr
ENST00000344644.9:c.855+55646T>A (UGT1A10)	ENSP00000343838.5:n.855+55646T>A
ENST00000354728.4:c.855+20234T>A (UGT1A9)	ENSP00000346768.4:n.855+20234T>A
ENST00000373424.5:c.-7-776T>A (UGT1A6)	ENSP00000362523.1:n.-7-776T>A
ENST00000373426.3:c.855+10231T>A (UGT1A7)	ENSP00000362525.3:n.855+10231T>A
ENST00000373445.1:c.855+55646T>A (UGT1A10)	ENSP00000362544.1:n.855+55646T>A
ENST00000373450.4:c.856-74011T>A (UGT1A8)	ENSP00000362549.4:n.856-74011T>A
ENST00000441351.1:c.19T>A (UGT1A6)	ENSP00000389637.1:p.Ser7Thr
ENST00000446481.6:c.-7-776T>A (UGT1A6)	ENSP00000401541.1:n.-7-776T>A
ENST00000480628.1:n.120-776T>A (UGT1A6)
NM_001072.3:c.19T>A (UGT1A6)	NP_001063.2:p.Ser7Thr
NM_019075.2:c.855+55646T>A (UGT1A10)	NP_061948.1:n.855+55646T>A
NM_019076.4:c.856-74011T>A (UGT1A8)	NP_061949.3:n.856-74011T>A
NM_019077.2:c.855+10231T>A (UGT1A7)	NP_061950.2:n.855+10231T>A
NM_021027.2:c.855+20234T>A (UGT1A9)	NP_066307.1:n.855+20234T>A
NM_205862.1:c.-7-776T>A (UGT1A6)	NP_995584.1:n.-7-776T>A
NM_001072.4:c.19T>A (UGT1A6) MANE Select	NP_001063.2:p.Ser7Thr
NM_021027.3:c.855+20234T>A (UGT1A9) MANE Select	NP_066307.1:n.855+20234T>A
NM_205862.2:c.-7-776T>A (UGT1A6)	NP_995584.1:n.-7-776T>A
NM_019075.4:c.855+55646T>A (UGT1A10) MANE Select	NP_061948.1:n.855+55646T>A
NM_019076.5:c.856-74011T>A (UGT1A8) MANE Select	NP_061949.3:n.856-74011T>A
NM_019077.3:c.855+10231T>A (UGT1A7) MANE Select	NP_061950.2:n.855+10231T>A
NM_205862.3:c.-7-776T>A (UGT1A6)	NP_995584.1:n.-7-776T>A