Canonical Allele Identifier: CA351071839

Gene: UGT1A10 UGT1A5 UGT1A7 UGT1A8 UGT1A3 UGT1A6 UGT1A1 UGT1A9 UGT1A4

Linked Data

• MyVariant Identifiers: chr2:g.234675721T>G (hg19) ; chr2:g.233767075T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233767075T>G , CM000664.2:g.233767075T>G	GRCh38
NC_000002.11:g.234675721T>G , CM000664.1:g.234675721T>G	GRCh37
NC_000002.10:g.234340460T>G	NCBI36
NG_002601.2:g.182332T>G
NG_033238.1:g.11803T>G , LRG_733:g.11803T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344644.10:c.897T>G (UGT1A10) MANE Select	ENSP00000343838.5:p.Ile299Met
ENST00000373414.4:c.909T>G (UGT1A5) MANE Select	ENSP00000362513.3:p.Ile303Met
ENST00000373426.4:c.897T>G (UGT1A7) MANE Select	ENSP00000362525.3:p.Ile299Met
ENST00000373450.5:c.897T>G (UGT1A8) MANE Select	ENSP00000362549.4:p.Ile299Met
ENST00000482026.6:c.909T>G (UGT1A3) MANE Select	ENSP00000418532.1:p.Ile303Met
ENST00000305139.11:c.903T>G (UGT1A6) MANE Select	ENSP00000303174.6:p.Ile301Met
ENST00000305208.10:c.906T>G (UGT1A1) MANE Select	ENSP00000304845.5:p.Ile302Met
ENST00000354728.5:c.897T>G (UGT1A9) MANE Select	ENSP00000346768.4:p.Ile299Met
ENST00000373409.8:c.909T>G (UGT1A4) MANE Select	ENSP00000362508.4:p.Ile303Met
ENST00000305139.10:c.903T>G (UGT1A6)	ENSP00000303174.6:p.Ile301Met
ENST00000305208.9:c.906T>G (UGT1A1)	ENSP00000304845.5:p.Ile302Met
ENST00000344644.9:c.897T>G (UGT1A10)	ENSP00000343838.5:p.Ile299Met
ENST00000354728.4:c.897T>G (UGT1A9)	ENSP00000346768.4:p.Ile299Met
ENST00000360418.4:c.906T>G (UGT1A1)	ENSP00000353593.3:p.Ile302Met
ENST00000373409.7:c.909T>G (UGT1A4)	ENSP00000362508.3:p.Ile303Met
ENST00000373414.3:c.909T>G	ENSP00000362513.3:p.Ile303Met
ENST00000373424.5:c.102T>G (UGT1A6)	ENSP00000362523.1:p.Ile34Met
ENST00000373426.3:c.897T>G (UGT1A7)	ENSP00000362525.3:p.Ile299Met
ENST00000373445.1:c.897T>G (UGT1A10)	ENSP00000362544.1:p.Ile299Met
ENST00000373450.4:c.897T>G (UGT1A8)	ENSP00000362549.4:p.Ile299Met
ENST00000406651.1:c.102T>G (UGT1A6)	ENSP00000386107.1:p.Ile34Met
ENST00000446481.6:c.102T>G (UGT1A6)	ENSP00000401541.1:p.Ile34Met
ENST00000450233.1:c.909T>G (UGT1A4)	ENSP00000408608.1:p.Ile303Met
ENST00000482026.5:c.909T>G	ENSP00000418532.1:p.Ile303Met
ENST00000484784.2:c.483T>G (UGT1A6)	ENSP00000419780.2:n.483T>G
NM_000463.2:c.906T>G , LRG_733t1:c.906T>G (UGT1A1)	NP_000454.1:p.Ile302Met
NM_001072.3:c.903T>G (UGT1A6)	NP_001063.2:p.Ile301Met
NM_007120.2:c.909T>G (UGT1A4)	NP_009051.1:p.Ile303Met
NM_019075.2:c.897T>G (UGT1A10)	NP_061948.1:p.Ile299Met
NM_019076.4:c.897T>G (UGT1A8)	NP_061949.3:p.Ile299Met
NM_019077.2:c.897T>G (UGT1A7)	NP_061950.2:p.Ile299Met
NM_019078.1:c.909T>G (UGT1A5)	NP_061951.1:p.Ile303Met
NM_019093.2:c.909T>G (UGT1A3)	NP_061966.1:p.Ile303Met
NM_021027.2:c.897T>G (UGT1A9)	NP_066307.1:p.Ile299Met
NM_205862.1:c.102T>G (UGT1A6)	NP_995584.1:p.Ile34Met
NM_001072.4:c.903T>G (UGT1A6) MANE Select	NP_001063.2:p.Ile301Met
NM_021027.3:c.897T>G (UGT1A9) MANE Select	NP_066307.1:p.Ile299Met
NM_000463.3:c.906T>G (UGT1A1) MANE Select	NP_000454.1:p.Ile302Met
NM_007120.3:c.909T>G (UGT1A4) MANE Select	NP_009051.1:p.Ile303Met
NM_019093.4:c.909T>G (UGT1A3) MANE Select	NP_061966.1:p.Ile303Met
NM_205862.2:c.102T>G (UGT1A6)	NP_995584.1:p.Ile34Met
NM_019075.4:c.897T>G (UGT1A10) MANE Select	NP_061948.1:p.Ile299Met
NM_019076.5:c.897T>G (UGT1A8) MANE Select	NP_061949.3:p.Ile299Met
NM_019077.3:c.897T>G (UGT1A7) MANE Select	NP_061950.2:p.Ile299Met
NM_019078.2:c.909T>G (UGT1A5) MANE Select	NP_061951.1:p.Ile303Met
NM_205862.3:c.102T>G (UGT1A6)	NP_995584.1:p.Ile34Met