Canonical Allele Identifier: CA2663719519
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

gnomAD v4: 2-233772796-GCC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233772797_233772798del , CM000664.2:g.233772797_233772798del GRCh38
NC_000002.11:g.234681443_234681444del , CM000664.1:g.234681443_234681444del GRCh37
NC_000002.10:g.234346182_234346183del NCBI36
NG_002601.2:g.188054_188055del
NG_033238.1:g.17525_17526del , LRG_733:g.17525_17526del
NG_051337.1:g.2136_2137del

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.10:c.*238_*239del (UGT1A10) MANE Select ENSP00000343838.5:n.*238_*239del
ENST00000373414.4:c.*238_*239del (UGT1A5) MANE Select ENSP00000362513.3:n.*238_*239del
ENST00000373426.4:c.*238_*239del (UGT1A7) MANE Select ENSP00000362525.3:n.*238_*239del
ENST00000373450.5:c.*238_*239del (UGT1A8) MANE Select ENSP00000362549.4:n.*238_*239del
ENST00000482026.6:c.*238_*239del (UGT1A3) MANE Select ENSP00000418532.1:n.*238_*239del
ENST00000305139.11:c.*238_*239del (UGT1A6) MANE Select ENSP00000303174.6:n.*238_*239del
ENST00000305208.10:c.*238_*239del (UGT1A1) MANE Select ENSP00000304845.5:n.*238_*239del
ENST00000354728.5:c.*238_*239del (UGT1A9) MANE Select ENSP00000346768.4:n.*238_*239del
ENST00000373409.8:c.*238_*239del (UGT1A4) MANE Select ENSP00000362508.4:n.*238_*239del
ENST00000305139.10:c.*238_*239del (UGT1A6) ENSP00000303174.6:n.*238_*239del
ENST00000305208.9:c.*238_*239del (UGT1A1) ENSP00000304845.5:n.*238_*239del
ENST00000344644.9:c.*238_*239del (UGT1A10) ENSP00000343838.5:n.*238_*239del
ENST00000354728.4:c.*238_*239del (UGT1A9) ENSP00000346768.4:n.*238_*239del
ENST00000373409.7:c.*238_*239del (UGT1A4) ENSP00000362508.3:n.*238_*239del
ENST00000373414.3:c.1843_1844del ENSP00000362513.3:n.1843_1844del
ENST00000373426.3:c.1831_1832del (UGT1A7) ENSP00000362525.3:n.1831_1832del
ENST00000373450.4:c.*238_*239del (UGT1A8) ENSP00000362549.4:n.*238_*239del
ENST00000450233.1:c.1977_1978del (UGT1A4) ENSP00000408608.1:n.1977_1978del
ENST00000482026.5:c.*238_*239del ENSP00000418532.1:n.*238_*239del
NM_000463.2:c.*238_*239del , LRG_733t1:c.*238_*239del (UGT1A1) NP_000454.1:n.*238_*239del
NM_001072.3:c.*238_*239del (UGT1A6) NP_001063.2:n.*238_*239del
NM_007120.2:c.*238_*239del (UGT1A4) NP_009051.1:n.*238_*239del
NM_019075.2:c.*238_*239del (UGT1A10) NP_061948.1:n.*238_*239del
NM_019076.4:c.*238_*239del (UGT1A8) NP_061949.3:n.*238_*239del
NM_019077.2:c.1831_1832del (UGT1A7) NP_061950.2:n.1831_1832del
NM_019078.1:c.1843_1844del (UGT1A5) NP_061951.1:n.1843_1844del
NM_019093.2:c.1843_1844del (UGT1A3) NP_061966.1:n.1843_1844del
NM_021027.2:c.*238_*239del (UGT1A9) NP_066307.1:n.*238_*239del
NM_205862.1:c.*238_*239del (UGT1A6) NP_995584.1:n.*238_*239del
NM_001072.4:c.*238_*239del (UGT1A6) MANE Select NP_001063.2:n.*238_*239del
NM_021027.3:c.*238_*239del (UGT1A9) MANE Select NP_066307.1:n.*238_*239del
NM_000463.3:c.*238_*239del (UGT1A1) MANE Select NP_000454.1:n.*238_*239del
NM_007120.3:c.*238_*239del (UGT1A4) MANE Select NP_009051.1:n.*238_*239del
NM_019093.4:c.*238_*239del (UGT1A3) MANE Select NP_061966.1:n.*238_*239del
NM_205862.2:c.*238_*239del (UGT1A6) NP_995584.1:n.*238_*239del
NM_019075.4:c.*238_*239del (UGT1A10) MANE Select NP_061948.1:n.*238_*239del
NM_019076.5:c.*238_*239del (UGT1A8) MANE Select NP_061949.3:n.*238_*239del
NM_019077.3:c.*238_*239del (UGT1A7) MANE Select NP_061950.2:n.*238_*239del
NM_019078.2:c.*238_*239del (UGT1A5) MANE Select NP_061951.1:n.*238_*239del
NM_205862.3:c.*238_*239del (UGT1A6) NP_995584.1:n.*238_*239del
Search 100 bp 5'
Search 100 bp 3'