Canonical Allele Identifier: CA1063754288

Gene: UGT2B17 UGT2B15

Linked Data

• gnomAD v3: 4-68559921-G-GTTTTTT
• gnomAD v4: 4-68559921-G-GTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559926_68559927insTTTTTT , CM000666.2:g.68559926_68559927insTTTTTT	GRCh38
NC_000004.11:g.69425644_69425645insTTTTTT , CM000666.1:g.69425644_69425645insTTTTTT	GRCh37
NC_000004.10:g.69108239_69108240insTTTTTT	NCBI36
NG_017033.1:g.13606_13607insAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+615_1005+616insAAAAAA (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+615_1005+616insAAAAAA
ENST00000684088.1:c.255+615_255+616insAAAAAA (UGT2B17)	ENSP00000507374.1:n.255+615_255+616insAAAAAA
ENST00000317746.2:c.1005+615_1005+616insAAAAAA (UGT2B17)	ENSP00000320401.2:n.1005+615_1005+616insAAAAAA
ENST00000616841.4:c.1733-22396_1733-22395insAAAAAA (UGT2B15)	ENSP00000482004.1:n.1733-22396_1733-22395insAAAAAA
NM_001077.3:c.1005+615_1005+616insAAAAAA (UGT2B17)	NP_001068.1:n.1005+615_1005+616insAAAAAA
XM_024454205.1:c.1005+615_1005+616insAAAAAA (UGT2B17)	XP_024309973.1:n.1005+615_1005+616insAAAAAA
NM_001077.4:c.1005+615_1005+616insAAAAAA (UGT2B17) MANE Select	NP_001068.1:n.1005+615_1005+616insAAAAAA