Canonical Allele Identifier: CA1335825596
Gene: UGT1A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618450_233618451delinsCA , CM000664.2:g.233618450_233618451delinsCA GRCh38
NC_000002.11:g.234527096_234527097delinsCA , CM000664.1:g.234527096_234527097delinsCA GRCh37
NC_000002.10:g.234191835_234191836delinsCA NCBI36
NG_002601.2:g.33707_33708delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000373450.5:c.743_744delinsCA MANE Select ENSP00000362549.4:p.Thr248=
ENST00000373450.4:c.743_744delinsCA ENSP00000362549.4:p.Thr248=
NM_019076.4:c.743_744delinsCA NP_061949.3:p.Thr248=
NM_019076.5:c.743_744delinsCA MANE Select NP_061949.3:p.Thr248=