Canonical Allele Identifier: CA1335860887

Gene: UGT1A10 UGT1A7 UGT1A8 UGT1A6 UGT1A9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233693615_233693616delinsCT , CM000664.2:g.233693615_233693616delinsCT	GRCh38
NC_000002.11:g.234602261_234602262delinsCT , CM000664.1:g.234602261_234602262delinsCT	GRCh37
NC_000002.10:g.234267000_234267001delinsCT	NCBI36
NG_002601.2:g.108872_108873delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.855+56238_855+56239delinsCT (UGT1A10) MANE Select	ENSP00000343838.5:n.855+56238_855+56239delinsCT
ENST00000373426.4:c.855+10823_855+10824delinsCT (UGT1A7) MANE Select	ENSP00000362525.3:n.855+10823_855+10824delinsCT
ENST00000373450.5:c.856-73419_856-73418delinsCT (UGT1A8) MANE Select	ENSP00000362549.4:n.856-73419_856-73418delinsCT
ENST00000305139.11:c.611_612delinsCT (UGT1A6) MANE Select	ENSP00000303174.6:p.Thr204=
ENST00000354728.5:c.855+20826_855+20827delinsCT (UGT1A9) MANE Select	ENSP00000346768.4:n.855+20826_855+20827delinsCT
ENST00000305139.10:c.611_612delinsCT (UGT1A6)	ENSP00000303174.6:p.Thr204=
ENST00000344644.9:c.855+56238_855+56239delinsCT (UGT1A10)	ENSP00000343838.5:n.855+56238_855+56239delinsCT
ENST00000354728.4:c.855+20826_855+20827delinsCT (UGT1A9)	ENSP00000346768.4:n.855+20826_855+20827delinsCT
ENST00000373424.5:c.-7-184_-7-183delinsCT (UGT1A6)	ENSP00000362523.1:n.-7-184_-7-183delinsCT
ENST00000373426.3:c.855+10823_855+10824delinsCT (UGT1A7)	ENSP00000362525.3:n.855+10823_855+10824delinsCT
ENST00000373445.1:c.855+56238_855+56239delinsCT (UGT1A10)	ENSP00000362544.1:n.855+56238_855+56239delinsCT
ENST00000373450.4:c.856-73419_856-73418delinsCT (UGT1A8)	ENSP00000362549.4:n.856-73419_856-73418delinsCT
ENST00000446481.6:c.-7-184_-7-183delinsCT (UGT1A6)	ENSP00000401541.1:n.-7-184_-7-183delinsCT
ENST00000480628.1:n.120-184_120-183delinsCT (UGT1A6)
NM_001072.3:c.611_612delinsCT (UGT1A6)	NP_001063.2:p.Thr204=
NM_019075.2:c.855+56238_855+56239delinsCT (UGT1A10)	NP_061948.1:n.855+56238_855+56239delinsCT
NM_019076.4:c.856-73419_856-73418delinsCT (UGT1A8)	NP_061949.3:n.856-73419_856-73418delinsCT
NM_019077.2:c.855+10823_855+10824delinsCT (UGT1A7)	NP_061950.2:n.855+10823_855+10824delinsCT
NM_021027.2:c.855+20826_855+20827delinsCT (UGT1A9)	NP_066307.1:n.855+20826_855+20827delinsCT
NM_205862.1:c.-7-184_-7-183delinsCT (UGT1A6)	NP_995584.1:n.-7-184_-7-183delinsCT
NM_001072.4:c.611_612delinsCT (UGT1A6) MANE Select	NP_001063.2:p.Thr204=
NM_021027.3:c.855+20826_855+20827delinsCT (UGT1A9) MANE Select	NP_066307.1:n.855+20826_855+20827delinsCT
NM_205862.2:c.-7-184_-7-183delinsCT (UGT1A6)	NP_995584.1:n.-7-184_-7-183delinsCT
NM_019075.4:c.855+56238_855+56239delinsCT (UGT1A10) MANE Select	NP_061948.1:n.855+56238_855+56239delinsCT
NM_019076.5:c.856-73419_856-73418delinsCT (UGT1A8) MANE Select	NP_061949.3:n.856-73419_856-73418delinsCT
NM_019077.3:c.855+10823_855+10824delinsCT (UGT1A7) MANE Select	NP_061950.2:n.855+10823_855+10824delinsCT
NM_205862.3:c.-7-184_-7-183delinsCT (UGT1A6)	NP_995584.1:n.-7-184_-7-183delinsCT