Canonical Allele Identifier: CA1335854569

Gene: UGT1A10 UGT1A8 UGT1A9

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233675757_233675758delinsCT , CM000664.2:g.233675757_233675758delinsCT	GRCh38
NC_000002.11:g.234584403_234584404delinsCT , CM000664.1:g.234584403_234584404delinsCT	GRCh37
NC_000002.10:g.234249142_234249143delinsCT	NCBI36
NG_002601.2:g.91014_91015delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.855+38380_855+38381delinsCT (UGT1A10) MANE Select	ENSP00000343838.5:n.855+38380_855+38381delinsCT
ENST00000373450.5:c.855+57195_855+57196delinsCT (UGT1A8) MANE Select	ENSP00000362549.4:n.855+57195_855+57196delinsCT
ENST00000354728.5:c.855+2968_855+2969delinsCT (UGT1A9) MANE Select	ENSP00000346768.4:n.855+2968_855+2969delinsCT
ENST00000344644.9:c.855+38380_855+38381delinsCT (UGT1A10)	ENSP00000343838.5:n.855+38380_855+38381delinsCT
ENST00000354728.4:c.855+2968_855+2969delinsCT (UGT1A9)	ENSP00000346768.4:n.855+2968_855+2969delinsCT
ENST00000373445.1:c.855+38380_855+38381delinsCT (UGT1A10)	ENSP00000362544.1:n.855+38380_855+38381delinsCT
ENST00000373450.4:c.855+57195_855+57196delinsCT (UGT1A8)	ENSP00000362549.4:n.855+57195_855+57196delinsCT
NM_019075.2:c.855+38380_855+38381delinsCT (UGT1A10)	NP_061948.1:n.855+38380_855+38381delinsCT
NM_019076.4:c.855+57195_855+57196delinsCT (UGT1A8)	NP_061949.3:n.855+57195_855+57196delinsCT
NM_021027.2:c.855+2968_855+2969delinsCT (UGT1A9)	NP_066307.1:n.855+2968_855+2969delinsCT
NM_021027.3:c.855+2968_855+2969delinsCT (UGT1A9) MANE Select	NP_066307.1:n.855+2968_855+2969delinsCT
NM_019075.4:c.855+38380_855+38381delinsCT (UGT1A10) MANE Select	NP_061948.1:n.855+38380_855+38381delinsCT
NM_019076.5:c.855+57195_855+57196delinsCT (UGT1A8) MANE Select	NP_061949.3:n.855+57195_855+57196delinsCT