Canonical Allele Identifier: CA2496048920

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799689_47799690delinsTC , CM000664.2:g.47799689_47799690delinsTC	GRCh38
NC_000002.11:g.48026828_48026829delinsTC , CM000664.1:g.48026828_48026829delinsTC	GRCh37
NC_000002.10:g.47880332_47880333delinsTC	NCBI36
NG_007111.1:g.21543_21544delinsTC , LRG_219:g.21543_21544delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.1409_1410delinsTC (MSH6)	ENSP00000406248.2:p.Phe470=
ENST00000420813.6:c.1409_1410delinsTC (MSH6)	ENSP00000390382.2:p.Phe470=
ENST00000455383.6:c.1409_1410delinsTC (MSH6)	ENSP00000397484.2:p.Phe470=
ENST00000700004.2:c.1706_1707delinsTC (MSH6)	ENSP00000514752.2:p.Phe569=
ENST00000699999.1:n.1790_1791delinsTC (MSH6)
ENST00000700000.1:c.1606+100_1606+101delinsTC (MSH6)	ENSP00000514749.1:n.1606+100_1606+101deli...
ENST00000700002.1:c.1712_1713delinsTC (MSH6)	ENSP00000514750.1:p.Phe571=
ENST00000700003.1:c.627+3626_627+3627delinsTC (MSH6)	ENSP00000514751.1:n.627+3626_627+3627deli...
ENST00000700004.1:c.863_864delinsTC (MSH6)	ENSP00000514752.1:p.Phe288=
ENST00000234420.11:c.1706_1707delinsTC (MSH6) MANE Select	ENSP00000234420.5:p.Phe569=
ENST00000540021.6:c.1316_1317delinsTC (MSH6)	ENSP00000446475.1:p.Phe439=
ENST00000652107.1:c.1409_1410delinsTC (MSH6)	ENSP00000498629.1:p.Phe470=
ENST00000673637.1:c.1409_1410delinsTC (MSH6)	ENSP00000501310.1:p.Phe470=
ENST00000234420.9:c.1706_1707delinsTC (MSH6)	ENSP00000234420.4:p.Phe569=
ENST00000405808.5:c.169+8505_169+8506delinsGA (FBXO11)	ENSP00000385127.1:n.169+8505_169+8506deli...
ENST00000434234.5:c.*124+8304_*124+8305delinsGA (FBXO11)	ENSP00000402692.1:n.*124+8304_*124+8305de...
ENST00000445503.5:c.*1053_*1054delinsTC (MSH6)	ENSP00000405294.1:n.*1053_*1054delinsTC
ENST00000538136.1:c.800_801delinsTC (MSH6)	ENSP00000438580.1:p.Phe267=
ENST00000540021.5:c.1316_1317delinsTC (MSH6)	ENSP00000446475.1:p.Phe439=
ENST00000614496.4:c.800_801delinsTC (MSH6)	ENSP00000477844.1:p.Phe267=
ENST00000616033.4:c.1703_1704delinsTC (MSH6)	ENSP00000480261.1:p.Phe568=
ENST00000622629.4:c.-1391_-1390delinsTC (MSH6)	ENSP00000482078.1:n.-1391_-1390delinsTC
NM_000179.2:c.1706_1707delinsTC , LRG_219t1:c.1706_1707delinsTC (MSH6)	NP_000170.1:p.Phe569=
NM_001281492.1:c.1316_1317delinsTC (MSH6)	NP_001268421.1:p.Phe439=
NM_001281493.1:c.800_801delinsTC (MSH6)	NP_001268422.1:p.Phe267=
NM_001281494.1:c.800_801delinsTC (MSH6)	NP_001268423.1:p.Phe267=
XM_005264271.1:c.1409_1410delinsTC (MSH6)	XP_005264328.1:p.Phe470=
XM_011532798.1:c.1523_1524delinsTC (MSH6)	XP_011531100.1:p.Phe508=
XM_011532799.1:c.1409_1410delinsTC (MSH6)	XP_011531101.1:p.Phe470=
XM_011532800.1:c.1409_1410delinsTC (MSH6)	XP_011531102.1:p.Phe470=
XM_024452819.1:c.1706_1707delinsTC (MSH6)	XP_024308587.1:p.Phe569=
XM_024452820.1:c.1523_1524delinsTC (MSH6)	XP_024308588.1:p.Phe508=
XM_024452821.1:c.1409_1410delinsTC (MSH6)	XP_024308589.1:p.Phe470=
XM_024452822.1:c.800_801delinsTC (MSH6)	XP_024308590.1:p.Phe267=
NM_000179.3:c.1706_1707delinsTC (MSH6) MANE Select	NP_000170.1:p.Phe569=
NM_001281492.2:c.1316_1317delinsTC (MSH6)	NP_001268421.1:p.Phe439=
NM_001281493.2:c.800_801delinsTC (MSH6)	NP_001268422.1:p.Phe267=
NM_001281494.2:c.800_801delinsTC (MSH6)	NP_001268423.1:p.Phe267=