Canonical Allele Identifier: CA351067930
Gene: UGT1A10 HGNC NCBI
UGT1A5 HGNC NCBI
UGT1A7 HGNC NCBI
UGT1A8 HGNC NCBI
UGT1A3 HGNC NCBI
UGT1A6 HGNC NCBI
UGT1A1 HGNC NCBI
UGT1A9 HGNC NCBI
UGT1A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.234669628C>G (hg19) chr2:g.233760982C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233760982C>G , CM000664.2:g.233760982C>G GRCh38
NC_000002.11:g.234669628C>G , CM000664.1:g.234669628C>G GRCh37
NC_000002.10:g.234334367C>G NCBI36
NG_002601.2:g.176239C>G
NG_033238.1:g.5710C>G , LRG_733:g.5710C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344644.10:c.856-6052C>G (UGT1A10) MANE Select ENSP00000343838.5:n.856-6052C>G
ENST00000373414.4:c.868-6052C>G (UGT1A5) MANE Select ENSP00000362513.3:n.868-6052C>G
ENST00000373426.4:c.856-6052C>G (UGT1A7) MANE Select ENSP00000362525.3:n.856-6052C>G
ENST00000373450.5:c.856-6052C>G (UGT1A8) MANE Select ENSP00000362549.4:n.856-6052C>G
ENST00000482026.6:c.868-6052C>G (UGT1A3) MANE Select ENSP00000418532.1:n.868-6052C>G
ENST00000305139.11:c.862-6052C>G (UGT1A6) MANE Select ENSP00000303174.6:n.862-6052C>G
ENST00000305208.10:c.695C>G (UGT1A1) MANE Select ENSP00000304845.5:p.Thr232Ser
ENST00000354728.5:c.856-6052C>G (UGT1A9) MANE Select ENSP00000346768.4:n.856-6052C>G
ENST00000373409.8:c.868-6052C>G (UGT1A4) MANE Select ENSP00000362508.4:n.868-6052C>G
ENST00000305139.10:c.862-6052C>G (UGT1A6) ENSP00000303174.6:n.862-6052C>G
ENST00000305208.9:c.695C>G (UGT1A1) ENSP00000304845.5:p.Thr232Ser
ENST00000344644.9:c.856-6052C>G (UGT1A10) ENSP00000343838.5:n.856-6052C>G
ENST00000354728.4:c.856-6052C>G (UGT1A9) ENSP00000346768.4:n.856-6052C>G
ENST00000360418.4:c.695C>G (UGT1A1) ENSP00000353593.3:p.Thr232Ser
ENST00000373409.7:c.868-6052C>G (UGT1A4) ENSP00000362508.3:n.868-6052C>G
ENST00000373414.3:c.868-6052C>G ENSP00000362513.3:n.868-6052C>G
ENST00000373424.5:c.61-6052C>G (UGT1A6) ENSP00000362523.1:n.61-6052C>G
ENST00000373426.3:c.856-6052C>G (UGT1A7) ENSP00000362525.3:n.856-6052C>G
ENST00000373445.1:c.856-6052C>G (UGT1A10) ENSP00000362544.1:n.856-6052C>G
ENST00000373450.4:c.856-6052C>G (UGT1A8) ENSP00000362549.4:n.856-6052C>G
ENST00000406651.1:c.61-6052C>G (UGT1A6) ENSP00000386107.1:n.61-6052C>G
ENST00000446481.6:c.61-6052C>G (UGT1A6) ENSP00000401541.1:n.61-6052C>G
ENST00000450233.1:c.868-6052C>G (UGT1A4) ENSP00000408608.1:n.868-6052C>G
ENST00000482026.5:c.868-6052C>G ENSP00000418532.1:n.868-6052C>G
ENST00000484784.2:c.442-6052C>G (UGT1A6) ENSP00000419780.2:n.442-6052C>G
NM_000463.2:c.695C>G , LRG_733t1:c.695C>G (UGT1A1) NP_000454.1:p.Thr232Ser
NM_001072.3:c.862-6052C>G (UGT1A6) NP_001063.2:n.862-6052C>G
NM_007120.2:c.868-6052C>G (UGT1A4) NP_009051.1:n.868-6052C>G
NM_019075.2:c.856-6052C>G (UGT1A10) NP_061948.1:n.856-6052C>G
NM_019076.4:c.856-6052C>G (UGT1A8) NP_061949.3:n.856-6052C>G
NM_019077.2:c.856-6052C>G (UGT1A7) NP_061950.2:n.856-6052C>G
NM_019078.1:c.868-6052C>G (UGT1A5) NP_061951.1:n.868-6052C>G
NM_019093.2:c.868-6052C>G (UGT1A3) NP_061966.1:n.868-6052C>G
NM_021027.2:c.856-6052C>G (UGT1A9) NP_066307.1:n.856-6052C>G
NM_205862.1:c.61-6052C>G (UGT1A6) NP_995584.1:n.61-6052C>G
NM_001072.4:c.862-6052C>G (UGT1A6) MANE Select NP_001063.2:n.862-6052C>G
NM_021027.3:c.856-6052C>G (UGT1A9) MANE Select NP_066307.1:n.856-6052C>G
NM_000463.3:c.695C>G (UGT1A1) MANE Select NP_000454.1:p.Thr232Ser
NM_007120.3:c.868-6052C>G (UGT1A4) MANE Select NP_009051.1:n.868-6052C>G
NM_019093.4:c.868-6052C>G (UGT1A3) MANE Select NP_061966.1:n.868-6052C>G
NM_205862.2:c.61-6052C>G (UGT1A6) NP_995584.1:n.61-6052C>G
NM_019075.4:c.856-6052C>G (UGT1A10) MANE Select NP_061948.1:n.856-6052C>G
NM_019076.5:c.856-6052C>G (UGT1A8) MANE Select NP_061949.3:n.856-6052C>G
NM_019077.3:c.856-6052C>G (UGT1A7) MANE Select NP_061950.2:n.856-6052C>G
NM_019078.2:c.868-6052C>G (UGT1A5) MANE Select NP_061951.1:n.868-6052C>G
NM_205862.3:c.61-6052C>G (UGT1A6) NP_995584.1:n.61-6052C>G
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