Canonical Allele Identifier: CA46706645

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs63750733
• MyVariant Identifiers: chr2:g.48025861_48025862insT (hg19) ; chr2:g.47798722_47798723insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798722_47798723insT , CM000664.2:g.47798722_47798723insT	GRCh38
NC_000002.11:g.48025861_48025862insT , CM000664.1:g.48025861_48025862insT	GRCh37
NC_000002.10:g.47879365_47879366insT	NCBI36
NG_007111.1:g.20576_20577insT , LRG_219:g.20576_20577insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.442_443insT (MSH6)	ENSP00000406248.2:p.Lys148IlefsTer9
ENST00000420813.6:c.442_443insT (MSH6)	ENSP00000390382.2:p.Lys148IlefsTer9
ENST00000455383.6:c.442_443insT (MSH6)	ENSP00000397484.2:p.Lys148IlefsTer9
ENST00000700004.2:c.739_740insT (MSH6)	ENSP00000514752.2:p.Lys247IlefsTer9
ENST00000699999.1:n.823_824insT (MSH6)
ENST00000700000.1:c.739_740insT (MSH6)	ENSP00000514749.1:p.Lys247IlefsTer9
ENST00000700002.1:c.745_746insT (MSH6)	ENSP00000514750.1:p.Lys249IlefsTer9
ENST00000700003.1:c.627+2659_627+2660insT (MSH6)	ENSP00000514751.1:n.627+2659_627+2660insT
ENST00000234420.11:c.739_740insT (MSH6) MANE Select	ENSP00000234420.5:p.Lys247IlefsTer9
ENST00000540021.6:c.349_350insT (MSH6)	ENSP00000446475.1:p.Lys117IlefsTer9
ENST00000652107.1:c.442_443insT (MSH6)	ENSP00000498629.1:p.Lys148IlefsTer9
ENST00000673637.1:c.442_443insT (MSH6)	ENSP00000501310.1:p.Lys148IlefsTer9
ENST00000673922.1:n.461_462insT (MSH6)
ENST00000234420.9:c.739_740insT (MSH6)	ENSP00000234420.4:p.Lys247IlefsTer9
ENST00000405808.5:c.170-9283_170-9282insA (FBXO11)	ENSP00000385127.1:n.170-9283_170-9282insA
ENST00000411819.1:c.442_443insT (MSH6)	ENSP00000406248.1:p.Lys148IlefsTer?
ENST00000434234.5:c.*124+9271_*124+9272insA (FBXO11)	ENSP00000402692.1:n.*124+9271_*124+9272insA
ENST00000445503.5:c.*86_*87insT (MSH6)	ENSP00000405294.1:n.*86_*87insT
ENST00000456246.1:c.*227_*228insT (MSH6)	ENSP00000410570.1:n.*227_*228insT
ENST00000538136.1:c.-168_-167insT (MSH6)	ENSP00000438580.1:n.-168_-167insT
ENST00000540021.5:c.349_350insT (MSH6)	ENSP00000446475.1:p.Lys117IlefsTer9
ENST00000614496.4:c.-168_-167insT (MSH6)	ENSP00000477844.1:n.-168_-167insT
ENST00000616033.4:c.736_737insT (MSH6)	ENSP00000480261.1:p.Lys246IlefsTer9
ENST00000622629.4:c.-2358_-2357insT (MSH6)	ENSP00000482078.1:n.-2358_-2357insT
NM_000179.2:c.739_740insT , LRG_219t1:c.739_740insT (MSH6)	NP_000170.1:p.Lys247IlefsTer9
NM_001281492.1:c.349_350insT (MSH6)	NP_001268421.1:p.Lys117IlefsTer9
NM_001281493.1:c.-168_-167insT (MSH6)	NP_001268422.1:n.-168_-167insT
NM_001281494.1:c.-168_-167insT (MSH6)	NP_001268423.1:n.-168_-167insT
XM_005264271.1:c.442_443insT (MSH6)	XP_005264328.1:p.Lys148IlefsTer9
XM_011532798.1:c.556_557insT (MSH6)	XP_011531100.1:p.Lys186IlefsTer9
XM_011532799.1:c.442_443insT (MSH6)	XP_011531101.1:p.Lys148IlefsTer9
XM_011532800.1:c.442_443insT (MSH6)	XP_011531102.1:p.Lys148IlefsTer9
XM_024452819.1:c.739_740insT (MSH6)	XP_024308587.1:p.Lys247IlefsTer9
XM_024452820.1:c.556_557insT (MSH6)	XP_024308588.1:p.Lys186IlefsTer9
XM_024452821.1:c.442_443insT (MSH6)	XP_024308589.1:p.Lys148IlefsTer9
XM_024452822.1:c.-168_-167insT (MSH6)	XP_024308590.1:n.-168_-167insT
NM_000179.3:c.739_740insT (MSH6) MANE Select	NP_000170.1:p.Lys247IlefsTer9
NM_001281492.2:c.349_350insT (MSH6)	NP_001268421.1:p.Lys117IlefsTer9
NM_001281493.2:c.-168_-167insT (MSH6)	NP_001268422.1:n.-168_-167insT
NM_001281494.2:c.-168_-167insT (MSH6)	NP_001268423.1:n.-168_-167insT