Canonical Allele Identifier: CA543530676

Gene: IL17RB ACTR8

Linked Data

• dbSNP Id: rs1442862793
• gnomAD v2: 3-53899201-GCT-G
• gnomAD v4: 3-53865174-GCT-G
• MyVariant Identifiers: chr3:g.53899202_53899203del (hg19) ; chr3:g.53865175_53865176del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53865178_53865179del , CM000665.2:g.53865178_53865179del	GRCh38
NC_000003.11:g.53899205_53899206del , CM000665.1:g.53899205_53899206del	GRCh37
NC_000003.10:g.53874245_53874246del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288167.8:c.1379_1380del (IL17RB) MANE Select	ENSP00000288167.3:p.Leu460GlnfsTer?
ENST00000288167.7:c.1379_1380del (IL17RB)	ENSP00000288167.3:p.Leu460GlnfsTer?
ENST00000475124.1:n.2412_2413del (IL17RB)
NM_018725.3:c.1379_1380del (IL17RB)	NP_061195.2:p.Leu460GlnfsTer?
XM_005265310.3:c.1466_1467del (IL17RB)	XP_005265367.1:p.Leu489GlnfsTer?
XM_005265311.3:c.1418_1419del (IL17RB)	XP_005265368.1:p.Leu473GlnfsTer?
XM_005265312.3:c.1331_1332del (IL17RB)	XP_005265369.1:p.Leu444GlnfsTer?
XM_005265587.3:c.*46-157_*46-156del (ACTR8)	XP_005265644.1:n.*46-157_*46-156del
XM_011533940.1:c.1115_1116del (IL17RB)	XP_011532242.1:p.Leu372GlnfsTer?
XR_245147.3:n.1680_1681del (IL17RB)
XR_940467.1:n.1545_1546del (IL17RB)
XR_940468.1:n.1458_1459del (IL17RB)
XM_005265310.5:c.1466_1467del (IL17RB)	XP_005265367.1:p.Leu489GlnfsTer?
XM_005265311.5:c.1418_1419del (IL17RB)	XP_005265368.1:p.Leu473GlnfsTer?
XM_005265312.5:c.1331_1332del (IL17RB)	XP_005265369.1:p.Leu444GlnfsTer?
XM_005265587.5:c.*46-157_*46-156del (ACTR8)	XP_005265644.1:n.*46-157_*46-156del
XM_011533941.3:c.*259_*260del (IL17RB)	XP_011532243.1:n.*259_*260del
XM_011534249.3:c.*3543_*3544del (ACTR8)	XP_011532551.1:n.*3543_*3544del
XM_017006804.2:c.1115_1116del (IL17RB)	XP_016862293.1:p.Leu372GlnfsTer?
XM_017006805.2:c.1067_1068del (IL17RB)	XP_016862294.1:p.Leu356GlnfsTer?
XM_017006806.2:c.1028_1029del (IL17RB)	XP_016862295.1:p.Leu343GlnfsTer?
XM_017006807.2:c.*259_*260del (IL17RB)	XP_016862296.1:n.*259_*260del
XR_940516.3:n.5496_5497del (ACTR8)
NM_018725.4:c.1379_1380del (IL17RB) MANE Select	NP_061195.2:p.Leu460GlnfsTer?