Canonical Allele Identifier: CA2496048994

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799782_47799784delinsATC , CM000664.2:g.47799782_47799784delinsATC	GRCh38
NC_000002.11:g.48026921_48026923delinsATC , CM000664.1:g.48026921_48026923delinsATC	GRCh37
NC_000002.10:g.47880425_47880427delinsATC	NCBI36
NG_007111.1:g.21636_21638delinsATC , LRG_219:g.21636_21638delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.1502_1504delinsATC (MSH6)	ENSP00000406248.2:p.Asn501=
ENST00000420813.6:c.1502_1504delinsATC (MSH6)	ENSP00000390382.2:p.Asn501=
ENST00000455383.6:c.1502_1504delinsATC (MSH6)	ENSP00000397484.2:p.Asn501=
ENST00000700004.2:c.1799_1801delinsATC (MSH6)	ENSP00000514752.2:p.Asn600=
ENST00000699999.1:n.1883_1885delinsATC (MSH6)
ENST00000700000.1:c.1606+193_1606+195delinsATC (MSH6)	ENSP00000514749.1:n.1606+193_1606+195delinsATC
ENST00000700002.1:c.1805_1807delinsATC (MSH6)	ENSP00000514750.1:p.Asn602=
ENST00000700003.1:c.628-3638_628-3636delinsATC (MSH6)	ENSP00000514751.1:n.628-3638_628-3636delinsATC
ENST00000700004.1:c.956_958delinsATC (MSH6)	ENSP00000514752.1:p.Asn319=
ENST00000234420.11:c.1799_1801delinsATC (MSH6) MANE Select	ENSP00000234420.5:p.Asn600=
ENST00000540021.6:c.1409_1411delinsATC (MSH6)	ENSP00000446475.1:p.Asn470=
ENST00000652107.1:c.1502_1504delinsATC (MSH6)	ENSP00000498629.1:p.Asn501=
ENST00000673637.1:c.1502_1504delinsATC (MSH6)	ENSP00000501310.1:p.Asn501=
ENST00000234420.9:c.1799_1801delinsATC (MSH6)	ENSP00000234420.4:p.Asn600=
ENST00000405808.5:c.169+8411_169+8413delinsGAT (FBXO11)	ENSP00000385127.1:n.169+8411_169+8413delinsGAT
ENST00000434234.5:c.*124+8210_*124+8212delinsGAT (FBXO11)	ENSP00000402692.1:n.*124+8210_*124+8212delinsGAT
ENST00000445503.5:c.*1146_*1148delinsATC (MSH6)	ENSP00000405294.1:n.*1146_*1148delinsATC
ENST00000538136.1:c.893_895delinsATC (MSH6)	ENSP00000438580.1:p.Asn298=
ENST00000540021.5:c.1409_1411delinsATC (MSH6)	ENSP00000446475.1:p.Asn470=
ENST00000614496.4:c.893_895delinsATC (MSH6)	ENSP00000477844.1:p.Asn298=
ENST00000616033.4:c.1796_1798delinsATC (MSH6)	ENSP00000480261.1:p.Asn599=
ENST00000622629.4:c.-1298_-1296delinsATC (MSH6)	ENSP00000482078.1:n.-1298_-1296delinsATC
NM_000179.2:c.1799_1801delinsATC , LRG_219t1:c.1799_1801delinsATC (MSH6)	NP_000170.1:p.Asn600=
NM_001281492.1:c.1409_1411delinsATC (MSH6)	NP_001268421.1:p.Asn470=
NM_001281493.1:c.893_895delinsATC (MSH6)	NP_001268422.1:p.Asn298=
NM_001281494.1:c.893_895delinsATC (MSH6)	NP_001268423.1:p.Asn298=
XM_005264271.1:c.1502_1504delinsATC (MSH6)	XP_005264328.1:p.Asn501=
XM_011532798.1:c.1616_1618delinsATC (MSH6)	XP_011531100.1:p.Asn539=
XM_011532799.1:c.1502_1504delinsATC (MSH6)	XP_011531101.1:p.Asn501=
XM_011532800.1:c.1502_1504delinsATC (MSH6)	XP_011531102.1:p.Asn501=
XM_024452819.1:c.1799_1801delinsATC (MSH6)	XP_024308587.1:p.Asn600=
XM_024452820.1:c.1616_1618delinsATC (MSH6)	XP_024308588.1:p.Asn539=
XM_024452821.1:c.1502_1504delinsATC (MSH6)	XP_024308589.1:p.Asn501=
XM_024452822.1:c.893_895delinsATC (MSH6)	XP_024308590.1:p.Asn298=
NM_000179.3:c.1799_1801delinsATC (MSH6) MANE Select	NP_000170.1:p.Asn600=
NM_001281492.2:c.1409_1411delinsATC (MSH6)	NP_001268421.1:p.Asn470=
NM_001281493.2:c.893_895delinsATC (MSH6)	NP_001268422.1:p.Asn298=
NM_001281494.2:c.893_895delinsATC (MSH6)	NP_001268423.1:p.Asn298=