Canonical Allele Identifier: CA1335894698

Gene: UGT1A10 UGT1A5 UGT1A7 UGT1A8 UGT1A3 UGT1A6 UGT1A1 UGT1A9 UGT1A4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233767045_233767046delinsCT , CM000664.2:g.233767045_233767046delinsCT	GRCh38
NC_000002.11:g.234675691_234675692delinsCT , CM000664.1:g.234675691_234675692delinsCT	GRCh37
NC_000002.10:g.234340430_234340431delinsCT	NCBI36
NG_002601.2:g.182302_182303delinsCT
NG_033238.1:g.11773_11774delinsCT , LRG_733:g.11773_11774delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.867_868delinsCT (UGT1A10) MANE Select	ENSP00000343838.5:p.Ala289=
ENST00000373414.4:c.879_880delinsCT (UGT1A5) MANE Select	ENSP00000362513.3:p.Ala293=
ENST00000373426.4:c.867_868delinsCT (UGT1A7) MANE Select	ENSP00000362525.3:p.Ala289=
ENST00000373450.5:c.867_868delinsCT (UGT1A8) MANE Select	ENSP00000362549.4:p.Ala289=
ENST00000482026.6:c.879_880delinsCT (UGT1A3) MANE Select	ENSP00000418532.1:p.Ala293=
ENST00000305139.11:c.873_874delinsCT (UGT1A6) MANE Select	ENSP00000303174.6:p.Ala291=
ENST00000305208.10:c.876_877delinsCT (UGT1A1) MANE Select	ENSP00000304845.5:p.Ala292=
ENST00000354728.5:c.867_868delinsCT (UGT1A9) MANE Select	ENSP00000346768.4:p.Ala289=
ENST00000373409.8:c.879_880delinsCT (UGT1A4) MANE Select	ENSP00000362508.4:p.Ala293=
ENST00000305139.10:c.873_874delinsCT (UGT1A6)	ENSP00000303174.6:p.Ala291=
ENST00000305208.9:c.876_877delinsCT (UGT1A1)	ENSP00000304845.5:p.Ala292=
ENST00000344644.9:c.867_868delinsCT (UGT1A10)	ENSP00000343838.5:p.Ala289=
ENST00000354728.4:c.867_868delinsCT (UGT1A9)	ENSP00000346768.4:p.Ala289=
ENST00000360418.4:c.876_877delinsCT (UGT1A1)	ENSP00000353593.3:p.Ala292=
ENST00000373409.7:c.879_880delinsCT (UGT1A4)	ENSP00000362508.3:p.Ala293=
ENST00000373414.3:c.879_880delinsCT	ENSP00000362513.3:p.Ala293=
ENST00000373424.5:c.72_73delinsCT (UGT1A6)	ENSP00000362523.1:p.Ala24=
ENST00000373426.3:c.867_868delinsCT (UGT1A7)	ENSP00000362525.3:p.Ala289=
ENST00000373445.1:c.867_868delinsCT (UGT1A10)	ENSP00000362544.1:p.Ala289=
ENST00000373450.4:c.867_868delinsCT (UGT1A8)	ENSP00000362549.4:p.Ala289=
ENST00000406651.1:c.72_73delinsCT (UGT1A6)	ENSP00000386107.1:p.Ala24=
ENST00000446481.6:c.72_73delinsCT (UGT1A6)	ENSP00000401541.1:p.Ala24=
ENST00000450233.1:c.879_880delinsCT (UGT1A4)	ENSP00000408608.1:p.Ala293=
ENST00000482026.5:c.879_880delinsCT	ENSP00000418532.1:p.Ala293=
ENST00000484784.2:c.453_454delinsCT (UGT1A6)	ENSP00000419780.2:n.453_454delinsCT
NM_000463.2:c.876_877delinsCT , LRG_733t1:c.876_877delinsCT (UGT1A1)	NP_000454.1:p.Ala292=
NM_001072.3:c.873_874delinsCT (UGT1A6)	NP_001063.2:p.Ala291=
NM_007120.2:c.879_880delinsCT (UGT1A4)	NP_009051.1:p.Ala293=
NM_019075.2:c.867_868delinsCT (UGT1A10)	NP_061948.1:p.Ala289=
NM_019076.4:c.867_868delinsCT (UGT1A8)	NP_061949.3:p.Ala289=
NM_019077.2:c.867_868delinsCT (UGT1A7)	NP_061950.2:p.Ala289=
NM_019078.1:c.879_880delinsCT (UGT1A5)	NP_061951.1:p.Ala293=
NM_019093.2:c.879_880delinsCT (UGT1A3)	NP_061966.1:p.Ala293=
NM_021027.2:c.867_868delinsCT (UGT1A9)	NP_066307.1:p.Ala289=
NM_205862.1:c.72_73delinsCT (UGT1A6)	NP_995584.1:p.Ala24=
NM_001072.4:c.873_874delinsCT (UGT1A6) MANE Select	NP_001063.2:p.Ala291=
NM_021027.3:c.867_868delinsCT (UGT1A9) MANE Select	NP_066307.1:p.Ala289=
NM_000463.3:c.876_877delinsCT (UGT1A1) MANE Select	NP_000454.1:p.Ala292=
NM_007120.3:c.879_880delinsCT (UGT1A4) MANE Select	NP_009051.1:p.Ala293=
NM_019093.4:c.879_880delinsCT (UGT1A3) MANE Select	NP_061966.1:p.Ala293=
NM_205862.2:c.72_73delinsCT (UGT1A6)	NP_995584.1:p.Ala24=
NM_019075.4:c.867_868delinsCT (UGT1A10) MANE Select	NP_061948.1:p.Ala289=
NM_019076.5:c.867_868delinsCT (UGT1A8) MANE Select	NP_061949.3:p.Ala289=
NM_019077.3:c.867_868delinsCT (UGT1A7) MANE Select	NP_061950.2:p.Ala289=
NM_019078.2:c.879_880delinsCT (UGT1A5) MANE Select	NP_061951.1:p.Ala293=
NM_205862.3:c.72_73delinsCT (UGT1A6)	NP_995584.1:p.Ala24=