Canonical Allele Identifier: CA2706083338

Gene: UGT2B17 UGT2B15

Linked Data

• dbSNP Id: rs2109771902

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559931_68559932insATTT , CM000666.2:g.68559931_68559932insATTT	GRCh38
NC_000004.11:g.69425649_69425650insATTT , CM000666.1:g.69425649_69425650insATTT	GRCh37
NC_000004.10:g.69108244_69108245insATTT	NCBI36
NG_017033.1:g.13599_13600insTAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+608_1005+609insTAAA (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+608_1005+609insTAAA
ENST00000684088.1:c.255+608_255+609insTAAA (UGT2B17)	ENSP00000507374.1:n.255+608_255+609insTAAA
ENST00000317746.2:c.1005+608_1005+609insTAAA (UGT2B17)	ENSP00000320401.2:n.1005+608_1005+609insTAAA
ENST00000616841.4:c.1733-22403_1733-22402insTAAA (UGT2B15)	ENSP00000482004.1:n.1733-22403_1733-22402insTAAA
NM_001077.3:c.1005+608_1005+609insTAAA (UGT2B17)	NP_001068.1:n.1005+608_1005+609insTAAA
XM_024454205.1:c.1005+608_1005+609insTAAA (UGT2B17)	XP_024309973.1:n.1005+608_1005+609insTAAA
NM_001077.4:c.1005+608_1005+609insTAAA (UGT2B17) MANE Select	NP_001068.1:n.1005+608_1005+609insTAAA