Canonical Allele Identifier: CA431958036

Gene: UGT1A10 UGT1A7 UGT1A8 UGT1A9

Linked Data

• dbSNP Id: rs776939121
• gnomAD v2: 2-234590880-G-C
• gnomAD v4: 2-233682234-G-C
• MyVariant Identifiers: chr2:g.234590880G>C (hg19) ; chr2:g.233682234G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233682234G>C , CM000664.2:g.233682234G>C	GRCh38
NC_000002.11:g.234590880G>C , CM000664.1:g.234590880G>C	GRCh37
NC_000002.10:g.234255619G>C	NCBI36
NG_002601.2:g.97491G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344644.10:c.855+44857G>C (UGT1A10) MANE Select	ENSP00000343838.5:n.855+44857G>C
ENST00000373426.4:c.297G>C (UGT1A7) MANE Select	ENSP00000362525.3:p.Thr99=
ENST00000373450.5:c.855+63672G>C (UGT1A8) MANE Select	ENSP00000362549.4:n.855+63672G>C
ENST00000354728.5:c.855+9445G>C (UGT1A9) MANE Select	ENSP00000346768.4:n.855+9445G>C
ENST00000344644.9:c.855+44857G>C (UGT1A10)	ENSP00000343838.5:n.855+44857G>C
ENST00000354728.4:c.855+9445G>C (UGT1A9)	ENSP00000346768.4:n.855+9445G>C
ENST00000373426.3:c.297G>C (UGT1A7)	ENSP00000362525.3:p.Thr99=
ENST00000373445.1:c.855+44857G>C (UGT1A10)	ENSP00000362544.1:n.855+44857G>C
ENST00000373450.4:c.855+63672G>C (UGT1A8)	ENSP00000362549.4:n.855+63672G>C
NM_019075.2:c.855+44857G>C (UGT1A10)	NP_061948.1:n.855+44857G>C
NM_019076.4:c.855+63672G>C (UGT1A8)	NP_061949.3:n.855+63672G>C
NM_019077.2:c.297G>C (UGT1A7)	NP_061950.2:p.Thr99=
NM_021027.2:c.855+9445G>C (UGT1A9)	NP_066307.1:n.855+9445G>C
NM_021027.3:c.855+9445G>C (UGT1A9) MANE Select	NP_066307.1:n.855+9445G>C
NM_019075.4:c.855+44857G>C (UGT1A10) MANE Select	NP_061948.1:n.855+44857G>C
NM_019076.5:c.855+63672G>C (UGT1A8) MANE Select	NP_061949.3:n.855+63672G>C
NM_019077.3:c.297G>C (UGT1A7) MANE Select	NP_061950.2:p.Thr99=