Canonical Allele Identifier: CA351076327

Gene: UGT1A10 UGT1A5 UGT1A7 UGT1A8 UGT1A3 UGT1A6 UGT1A1 UGT1A9 UGT1A4

Linked Data

• gnomAD v4: 2-233772368-G-C
• MyVariant Identifiers: chr2:g.234681014G>C (hg19) ; chr2:g.233772368G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233772368G>C , CM000664.2:g.233772368G>C	GRCh38
NC_000002.11:g.234681014G>C , CM000664.1:g.234681014G>C	GRCh37
NC_000002.10:g.234345753G>C	NCBI36
NG_002601.2:g.187625G>C
NG_033238.1:g.17096G>C , LRG_733:g.17096G>C
NG_051337.1:g.1707G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.1402G>C (UGT1A10) MANE Select	ENSP00000343838.5:p.Ala468Pro
ENST00000373414.4:c.1414G>C (UGT1A5) MANE Select	ENSP00000362513.3:p.Ala472Pro
ENST00000373426.4:c.1402G>C (UGT1A7) MANE Select	ENSP00000362525.3:p.Ala468Pro
ENST00000373450.5:c.1402G>C (UGT1A8) MANE Select	ENSP00000362549.4:p.Ala468Pro
ENST00000482026.6:c.1414G>C (UGT1A3) MANE Select	ENSP00000418532.1:p.Ala472Pro
ENST00000305139.11:c.1408G>C (UGT1A6) MANE Select	ENSP00000303174.6:p.Ala470Pro
ENST00000305208.10:c.1411G>C (UGT1A1) MANE Select	ENSP00000304845.5:p.Ala471Pro
ENST00000354728.5:c.1402G>C (UGT1A9) MANE Select	ENSP00000346768.4:p.Ala468Pro
ENST00000373409.8:c.1414G>C (UGT1A4) MANE Select	ENSP00000362508.4:p.Ala472Pro
ENST00000305139.10:c.1408G>C (UGT1A6)	ENSP00000303174.6:p.Ala470Pro
ENST00000305208.9:c.1411G>C (UGT1A1)	ENSP00000304845.5:p.Ala471Pro
ENST00000344644.9:c.1402G>C (UGT1A10)	ENSP00000343838.5:p.Ala468Pro
ENST00000354728.4:c.1402G>C (UGT1A9)	ENSP00000346768.4:p.Ala468Pro
ENST00000373409.7:c.1414G>C (UGT1A4)	ENSP00000362508.3:p.Ala472Pro
ENST00000373414.3:c.1414G>C	ENSP00000362513.3:p.Ala472Pro
ENST00000373424.5:c.607G>C (UGT1A6)	ENSP00000362523.1:p.Ala203Pro
ENST00000373426.3:c.1402G>C (UGT1A7)	ENSP00000362525.3:p.Ala468Pro
ENST00000373450.4:c.1402G>C (UGT1A8)	ENSP00000362549.4:p.Ala468Pro
ENST00000450233.1:c.1548G>C (UGT1A4)	ENSP00000408608.1:n.1548G>C
ENST00000482026.5:c.1414G>C	ENSP00000418532.1:p.Ala472Pro
NM_000463.2:c.1411G>C , LRG_733t1:c.1411G>C (UGT1A1)	NP_000454.1:p.Ala471Pro
NM_001072.3:c.1408G>C (UGT1A6)	NP_001063.2:p.Ala470Pro
NM_007120.2:c.1414G>C (UGT1A4)	NP_009051.1:p.Ala472Pro
NM_019075.2:c.1402G>C (UGT1A10)	NP_061948.1:p.Ala468Pro
NM_019076.4:c.1402G>C (UGT1A8)	NP_061949.3:p.Ala468Pro
NM_019077.2:c.1402G>C (UGT1A7)	NP_061950.2:p.Ala468Pro
NM_019078.1:c.1414G>C (UGT1A5)	NP_061951.1:p.Ala472Pro
NM_019093.2:c.1414G>C (UGT1A3)	NP_061966.1:p.Ala472Pro
NM_021027.2:c.1402G>C (UGT1A9)	NP_066307.1:p.Ala468Pro
NM_205862.1:c.607G>C (UGT1A6)	NP_995584.1:p.Ala203Pro
NM_001072.4:c.1408G>C (UGT1A6) MANE Select	NP_001063.2:p.Ala470Pro
NM_021027.3:c.1402G>C (UGT1A9) MANE Select	NP_066307.1:p.Ala468Pro
NM_000463.3:c.1411G>C (UGT1A1) MANE Select	NP_000454.1:p.Ala471Pro
NM_007120.3:c.1414G>C (UGT1A4) MANE Select	NP_009051.1:p.Ala472Pro
NM_019093.4:c.1414G>C (UGT1A3) MANE Select	NP_061966.1:p.Ala472Pro
NM_205862.2:c.607G>C (UGT1A6)	NP_995584.1:p.Ala203Pro
NM_019075.4:c.1402G>C (UGT1A10) MANE Select	NP_061948.1:p.Ala468Pro
NM_019076.5:c.1402G>C (UGT1A8) MANE Select	NP_061949.3:p.Ala468Pro
NM_019077.3:c.1402G>C (UGT1A7) MANE Select	NP_061950.2:p.Ala468Pro
NM_019078.2:c.1414G>C (UGT1A5) MANE Select	NP_061951.1:p.Ala472Pro
NM_205862.3:c.607G>C (UGT1A6)	NP_995584.1:p.Ala203Pro