Canonical Allele Identifier: CA1465760670
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68559683_68559685delinsCAA , CM000666.2:g.68559683_68559685delinsCAA GRCh38
NC_000004.11:g.69425401_69425403delinsCAA , CM000666.1:g.69425401_69425403delinsCAA GRCh37
NC_000004.10:g.69107996_69107998delinsCAA NCBI36
NG_017033.1:g.13843_13845delinsTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000317746.3:c.1005+852_1005+854delinsTTG (UGT2B17) MANE Select ENSP00000320401.2:n.1005+852_1005+854deli...
ENST00000684088.1:c.255+852_255+854delinsTTG (UGT2B17) ENSP00000507374.1:n.255+852_255+854delins...
ENST00000317746.2:c.1005+852_1005+854delinsTTG (UGT2B17) ENSP00000320401.2:n.1005+852_1005+854deli...
ENST00000616841.4:c.1733-22159_1733-22157delinsTTG (UGT2B15) ENSP00000482004.1:n.1733-22159_1733-22157...
NM_001077.3:c.1005+852_1005+854delinsTTG (UGT2B17) NP_001068.1:n.1005+852_1005+854delinsTTG
XM_024454205.1:c.1005+852_1005+854delinsTTG (UGT2B17) XP_024309973.1:n.1005+852_1005+854delinsT...
NM_001077.4:c.1005+852_1005+854delinsTTG (UGT2B17) MANE Select NP_001068.1:n.1005+852_1005+854delinsTTG
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