Canonical Allele Identifier: CA1335844041

Gene: UGT1A10 UGT1A8

Linked Data

• dbSNP Id: rs2073860160

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233656668T>C , CM000664.2:g.233656668T>C	GRCh38
NC_000002.11:g.234565314T>C , CM000664.1:g.234565314T>C	GRCh37
NC_000002.10:g.234230053T>C	NCBI36
NG_002601.2:g.71925T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344644.10:c.855+19291T>C (UGT1A10) MANE Select	ENSP00000343838.5:n.855+19291T>C
ENST00000373450.5:c.855+38106T>C (UGT1A8) MANE Select	ENSP00000362549.4:n.855+38106T>C
ENST00000344644.9:c.855+19291T>C (UGT1A10)	ENSP00000343838.5:n.855+19291T>C
ENST00000373445.1:c.855+19291T>C (UGT1A10)	ENSP00000362544.1:n.855+19291T>C
ENST00000373450.4:c.855+38106T>C (UGT1A8)	ENSP00000362549.4:n.855+38106T>C
NM_019075.2:c.855+19291T>C (UGT1A10)	NP_061948.1:n.855+19291T>C
NM_019076.4:c.855+38106T>C (UGT1A8)	NP_061949.3:n.855+38106T>C
NM_019075.4:c.855+19291T>C (UGT1A10) MANE Select	NP_061948.1:n.855+19291T>C
NM_019076.5:c.855+38106T>C (UGT1A8) MANE Select	NP_061949.3:n.855+38106T>C