Canonical Allele Identifier: CA2599720449
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI

Linked Data

gnomAD v3: 4-68559925-T-TTTTG
gnomAD v4: 4-68559925-T-TTTTG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68559926_68559927insTTGT , CM000666.2:g.68559926_68559927insTTGT GRCh38
NC_000004.11:g.69425644_69425645insTTGT , CM000666.1:g.69425644_69425645insTTGT GRCh37
NC_000004.10:g.69108239_69108240insTTGT NCBI36
NG_017033.1:g.13602_13603insCAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000317746.3:c.1005+611_1005+612insCAAA (UGT2B17) MANE Select ENSP00000320401.2:n.1005+611_1005+612insCAAA
ENST00000684088.1:c.255+611_255+612insCAAA (UGT2B17) ENSP00000507374.1:n.255+611_255+612insCAAA
ENST00000317746.2:c.1005+611_1005+612insCAAA (UGT2B17) ENSP00000320401.2:n.1005+611_1005+612insCAAA
ENST00000616841.4:c.1733-22400_1733-22399insCAAA (UGT2B15) ENSP00000482004.1:n.1733-22400_1733-22399insCAAA
NM_001077.3:c.1005+611_1005+612insCAAA (UGT2B17) NP_001068.1:n.1005+611_1005+612insCAAA
XM_024454205.1:c.1005+611_1005+612insCAAA (UGT2B17) XP_024309973.1:n.1005+611_1005+612insCAAA
NM_001077.4:c.1005+611_1005+612insCAAA (UGT2B17) MANE Select NP_001068.1:n.1005+611_1005+612insCAAA
Search 100 bp 5'
Search 100 bp 3'