Canonical Allele Identifier: CA2580066070

Linked Data

ClinVar Variation Id: 2428588
ClinVar RCV Id: RCV003120189

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233693022_233693023delinsTG , CM000664.2:g.233693022_233693023delinsTG GRCh38
NC_000002.11:g.234601668_234601669delinsTG , CM000664.1:g.234601668_234601669delinsTG GRCh37
NC_000002.10:g.234266407_234266408delinsTG NCBI36
NG_002601.2:g.108279_108280delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.10:c.855+55645_855+55646delinsTG (UGT1A10) MANE Select ENSP00000343838.5:n.855+55645_855+55646de...
ENST00000373426.4:c.855+10230_855+10231delinsTG (UGT1A7) MANE Select ENSP00000362525.3:n.855+10230_855+10231de...
ENST00000373450.5:c.856-74012_856-74011delinsTG (UGT1A8) MANE Select ENSP00000362549.4:n.856-74012_856-74011de...
ENST00000305139.11:c.18_19delinsTG (UGT1A6) MANE Select ENSP00000303174.6:p.Ser7Ala
ENST00000354728.5:c.855+20233_855+20234delinsTG (UGT1A9) MANE Select ENSP00000346768.4:n.855+20233_855+20234de...
ENST00000305139.10:c.18_19delinsTG (UGT1A6) ENSP00000303174.6:p.Ser7Ala
ENST00000344644.9:c.855+55645_855+55646delinsTG (UGT1A10) ENSP00000343838.5:n.855+55645_855+55646de...
ENST00000354728.4:c.855+20233_855+20234delinsTG (UGT1A9) ENSP00000346768.4:n.855+20233_855+20234de...
ENST00000373424.5:c.-7-777_-7-776delinsTG (UGT1A6) ENSP00000362523.1:n.-7-777_-7-776delinsTG...
ENST00000373426.3:c.855+10230_855+10231delinsTG (UGT1A7) ENSP00000362525.3:n.855+10230_855+10231de...
ENST00000373445.1:c.855+55645_855+55646delinsTG (UGT1A10) ENSP00000362544.1:n.855+55645_855+55646de...
ENST00000373450.4:c.856-74012_856-74011delinsTG (UGT1A8) ENSP00000362549.4:n.856-74012_856-74011de...
ENST00000441351.1:c.18_19delinsTG (UGT1A6) ENSP00000389637.1:p.Ser7Ala
ENST00000446481.6:c.-7-777_-7-776delinsTG (UGT1A6) ENSP00000401541.1:n.-7-777_-7-776delinsTG...
ENST00000480628.1:n.120-777_120-776delinsTG (UGT1A6)
NM_001072.3:c.18_19delinsTG (UGT1A6) NP_001063.2:p.Ser7Ala
NM_019075.2:c.855+55645_855+55646delinsTG (UGT1A10) NP_061948.1:n.855+55645_855+55646delinsTG...
NM_019076.4:c.856-74012_856-74011delinsTG (UGT1A8) NP_061949.3:n.856-74012_856-74011delinsTG...
NM_019077.2:c.855+10230_855+10231delinsTG (UGT1A7) NP_061950.2:n.855+10230_855+10231delinsTG...
NM_021027.2:c.855+20233_855+20234delinsTG (UGT1A9) NP_066307.1:n.855+20233_855+20234delinsTG...
NM_205862.1:c.-7-777_-7-776delinsTG (UGT1A6) NP_995584.1:n.-7-777_-7-776delinsTG
NM_001072.4:c.18_19delinsTG (UGT1A6) MANE Select NP_001063.2:p.Ser7Ala
NM_021027.3:c.855+20233_855+20234delinsTG (UGT1A9) MANE Select NP_066307.1:n.855+20233_855+20234delinsTG...
NM_205862.2:c.-7-777_-7-776delinsTG (UGT1A6) NP_995584.1:n.-7-777_-7-776delinsTG
NM_019075.4:c.855+55645_855+55646delinsTG (UGT1A10) MANE Select NP_061948.1:n.855+55645_855+55646delinsTG...
NM_019076.5:c.856-74012_856-74011delinsTG (UGT1A8) MANE Select NP_061949.3:n.856-74012_856-74011delinsTG...
NM_019077.3:c.855+10230_855+10231delinsTG (UGT1A7) MANE Select NP_061950.2:n.855+10230_855+10231delinsTG...
NM_205862.3:c.-7-777_-7-776delinsTG (UGT1A6) NP_995584.1:n.-7-777_-7-776delinsTG