Canonical Allele Identifier: CA1335854498

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233675547_233675549delinsGGC , CM000664.2:g.233675547_233675549delinsGGC GRCh38
NC_000002.11:g.234584193_234584195delinsGGC , CM000664.1:g.234584193_234584195delinsGGC GRCh37
NC_000002.10:g.234248932_234248934delinsGGC NCBI36
NG_002601.2:g.90804_90806delinsGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000344644.10:c.855+38170_855+38172delinsGGC (UGT1A10) MANE Select ENSP00000343838.5:n.855+38170_855+38172de...
ENST00000373450.5:c.855+56985_855+56987delinsGGC (UGT1A8) MANE Select ENSP00000362549.4:n.855+56985_855+56987de...
ENST00000354728.5:c.855+2758_855+2760delinsGGC (UGT1A9) MANE Select ENSP00000346768.4:n.855+2758_855+2760deli...
ENST00000344644.9:c.855+38170_855+38172delinsGGC (UGT1A10) ENSP00000343838.5:n.855+38170_855+38172de...
ENST00000354728.4:c.855+2758_855+2760delinsGGC (UGT1A9) ENSP00000346768.4:n.855+2758_855+2760deli...
ENST00000373445.1:c.855+38170_855+38172delinsGGC (UGT1A10) ENSP00000362544.1:n.855+38170_855+38172de...
ENST00000373450.4:c.855+56985_855+56987delinsGGC (UGT1A8) ENSP00000362549.4:n.855+56985_855+56987de...
NM_019075.2:c.855+38170_855+38172delinsGGC (UGT1A10) NP_061948.1:n.855+38170_855+38172delinsGG...
NM_019076.4:c.855+56985_855+56987delinsGGC (UGT1A8) NP_061949.3:n.855+56985_855+56987delinsGG...
NM_021027.2:c.855+2758_855+2760delinsGGC (UGT1A9) NP_066307.1:n.855+2758_855+2760delinsGGC
NM_021027.3:c.855+2758_855+2760delinsGGC (UGT1A9) MANE Select NP_066307.1:n.855+2758_855+2760delinsGGC
NM_019075.4:c.855+38170_855+38172delinsGGC (UGT1A10) MANE Select NP_061948.1:n.855+38170_855+38172delinsGG...
NM_019076.5:c.855+56985_855+56987delinsGGC (UGT1A8) MANE Select NP_061949.3:n.855+56985_855+56987delinsGG...