Canonical Allele Identifier: CA2508795984
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68567239_68567243del , CM000666.2:g.68567239_68567243del GRCh38
NC_000004.11:g.69432957_69432961del , CM000666.1:g.69432957_69432961del GRCh37
NC_000004.10:g.69115552_69115556del NCBI36
NG_017033.1:g.6286_6290del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317746.3:c.724+519_724+523del (UGT2B17) MANE Select ENSP00000320401.2:n.724+519_724+523del
ENST00000684088.1:c.-26-1522_-26-1518del (UGT2B17) ENSP00000507374.1:n.-26-1522_-26-1518del
ENST00000317746.2:c.724+519_724+523del (UGT2B17) ENSP00000320401.2:n.724+519_724+523del
ENST00000616841.4:c.1733-29716_1733-29712del (UGT2B15) ENSP00000482004.1:n.1733-29716_1733-29712del
NM_001077.3:c.724+519_724+523del (UGT2B17) NP_001068.1:n.724+519_724+523del
XM_024454205.1:c.724+519_724+523del (UGT2B17) XP_024309973.1:n.724+519_724+523del
NM_001077.4:c.724+519_724+523del (UGT2B17) MANE Select NP_001068.1:n.724+519_724+523del
Search 100 bp 5'
Search 100 bp 3'