Canonical Allele Identifier: CA1465760805

Gene: UGT2B17 UGT2B15

Linked Data

• dbSNP Id: rs1731069858

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559800_68559801del , CM000666.2:g.68559800_68559801del	GRCh38
NC_000004.11:g.69425518_69425519del , CM000666.1:g.69425518_69425519del	GRCh37
NC_000004.10:g.69108113_69108114del	NCBI36
NG_017033.1:g.13728_13729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+737_1005+738del (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+737_1005+738del
ENST00000684088.1:c.255+737_255+738del (UGT2B17)	ENSP00000507374.1:n.255+737_255+738del
ENST00000317746.2:c.1005+737_1005+738del (UGT2B17)	ENSP00000320401.2:n.1005+737_1005+738del
ENST00000616841.4:c.1733-22274_1733-22273del (UGT2B15)	ENSP00000482004.1:n.1733-22274_1733-22273del
NM_001077.3:c.1005+737_1005+738del (UGT2B17)	NP_001068.1:n.1005+737_1005+738del
XM_024454205.1:c.1005+737_1005+738del (UGT2B17)	XP_024309973.1:n.1005+737_1005+738del
NM_001077.4:c.1005+737_1005+738del (UGT2B17) MANE Select	NP_001068.1:n.1005+737_1005+738del