Canonical Allele Identifier: CA1335860620

Gene: UGT1A10 UGT1A7 UGT1A8 UGT1A6 UGT1A9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233692971_233692973delinsCTT , CM000664.2:g.233692971_233692973delinsCTT	GRCh38
NC_000002.11:g.234601617_234601619delinsCTT , CM000664.1:g.234601617_234601619delinsCTT	GRCh37
NC_000002.10:g.234266356_234266358delinsCTT	NCBI36
NG_002601.2:g.108228_108230delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.855+55594_855+55596delinsCTT (UGT1A10) MANE Select	ENSP00000343838.5:n.855+55594_855+55596delinsCTT
ENST00000373426.4:c.855+10179_855+10181delinsCTT (UGT1A7) MANE Select	ENSP00000362525.3:n.855+10179_855+10181delinsCTT
ENST00000373450.5:c.856-74063_856-74061delinsCTT (UGT1A8) MANE Select	ENSP00000362549.4:n.856-74063_856-74061delinsCTT
ENST00000305139.11:c.-34_-32delinsCTT (UGT1A6) MANE Select	ENSP00000303174.6:n.-34_-32delinsCTT
ENST00000354728.5:c.855+20182_855+20184delinsCTT (UGT1A9) MANE Select	ENSP00000346768.4:n.855+20182_855+20184delinsCTT
ENST00000305139.10:c.-34_-32delinsCTT (UGT1A6)	ENSP00000303174.6:n.-34_-32delinsCTT
ENST00000344644.9:c.855+55594_855+55596delinsCTT (UGT1A10)	ENSP00000343838.5:n.855+55594_855+55596delinsCTT
ENST00000354728.4:c.855+20182_855+20184delinsCTT (UGT1A9)	ENSP00000346768.4:n.855+20182_855+20184delinsCTT
ENST00000373424.5:c.-7-828_-7-826delinsCTT (UGT1A6)	ENSP00000362523.1:n.-7-828_-7-826delinsCTT
ENST00000373426.3:c.855+10179_855+10181delinsCTT (UGT1A7)	ENSP00000362525.3:n.855+10179_855+10181delinsCTT
ENST00000373445.1:c.855+55594_855+55596delinsCTT (UGT1A10)	ENSP00000362544.1:n.855+55594_855+55596delinsCTT
ENST00000373450.4:c.856-74063_856-74061delinsCTT (UGT1A8)	ENSP00000362549.4:n.856-74063_856-74061delinsCTT
ENST00000441351.1:c.-1-33_-1-31delinsCTT (UGT1A6)	ENSP00000389637.1:n.-1-33_-1-31delinsCTT
ENST00000446481.6:c.-7-828_-7-826delinsCTT (UGT1A6)	ENSP00000401541.1:n.-7-828_-7-826delinsCTT
ENST00000480628.1:n.120-828_120-826delinsCTT (UGT1A6)
NM_001072.3:c.-34_-32delinsCTT (UGT1A6)	NP_001063.2:n.-34_-32delinsCTT
NM_019075.2:c.855+55594_855+55596delinsCTT (UGT1A10)	NP_061948.1:n.855+55594_855+55596delinsCTT
NM_019076.4:c.856-74063_856-74061delinsCTT (UGT1A8)	NP_061949.3:n.856-74063_856-74061delinsCTT
NM_019077.2:c.855+10179_855+10181delinsCTT (UGT1A7)	NP_061950.2:n.855+10179_855+10181delinsCTT
NM_021027.2:c.855+20182_855+20184delinsCTT (UGT1A9)	NP_066307.1:n.855+20182_855+20184delinsCTT
NM_205862.1:c.-7-828_-7-826delinsCTT (UGT1A6)	NP_995584.1:n.-7-828_-7-826delinsCTT
NM_001072.4:c.-34_-32delinsCTT (UGT1A6) MANE Select	NP_001063.2:n.-34_-32delinsCTT
NM_021027.3:c.855+20182_855+20184delinsCTT (UGT1A9) MANE Select	NP_066307.1:n.855+20182_855+20184delinsCTT
NM_205862.2:c.-7-828_-7-826delinsCTT (UGT1A6)	NP_995584.1:n.-7-828_-7-826delinsCTT
NM_019075.4:c.855+55594_855+55596delinsCTT (UGT1A10) MANE Select	NP_061948.1:n.855+55594_855+55596delinsCTT
NM_019076.5:c.856-74063_856-74061delinsCTT (UGT1A8) MANE Select	NP_061949.3:n.856-74063_856-74061delinsCTT
NM_019077.3:c.855+10179_855+10181delinsCTT (UGT1A7) MANE Select	NP_061950.2:n.855+10179_855+10181delinsCTT
NM_205862.3:c.-7-828_-7-826delinsCTT (UGT1A6)	NP_995584.1:n.-7-828_-7-826delinsCTT