Canonical Allele Identifier: CA1465760804

Gene: UGT2B17 UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559798_68559800delinsCTT , CM000666.2:g.68559798_68559800delinsCTT	GRCh38
NC_000004.11:g.69425516_69425518delinsCTT , CM000666.1:g.69425516_69425518delinsCTT	GRCh37
NC_000004.10:g.69108111_69108113delinsCTT	NCBI36
NG_017033.1:g.13728_13730delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+737_1005+739delinsAAG (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+737_1005+739delinsAAG
ENST00000684088.1:c.255+737_255+739delinsAAG (UGT2B17)	ENSP00000507374.1:n.255+737_255+739delinsAAG
ENST00000317746.2:c.1005+737_1005+739delinsAAG (UGT2B17)	ENSP00000320401.2:n.1005+737_1005+739delinsAAG
ENST00000616841.4:c.1733-22274_1733-22272delinsAAG (UGT2B15)	ENSP00000482004.1:n.1733-22274_1733-22272delinsAAG
NM_001077.3:c.1005+737_1005+739delinsAAG (UGT2B17)	NP_001068.1:n.1005+737_1005+739delinsAAG
XM_024454205.1:c.1005+737_1005+739delinsAAG (UGT2B17)	XP_024309973.1:n.1005+737_1005+739delinsAAG
NM_001077.4:c.1005+737_1005+739delinsAAG (UGT2B17) MANE Select	NP_001068.1:n.1005+737_1005+739delinsAAG