Canonical Allele Identifier: CA2496048136

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798756_47798759delinsTTGG , CM000664.2:g.47798756_47798759delinsTTGG	GRCh38
NC_000002.11:g.48025895_48025898delinsTTGG , CM000664.1:g.48025895_48025898delinsTTGG	GRCh37
NC_000002.10:g.47879399_47879402delinsTTGG	NCBI36
NG_007111.1:g.20610_20613delinsTTGG , LRG_219:g.20610_20613delinsTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.476_479delinsTTGG (MSH6)	ENSP00000406248.2:p.Ile159=
ENST00000420813.6:c.476_479delinsTTGG (MSH6)	ENSP00000390382.2:p.Ile159=
ENST00000455383.6:c.476_479delinsTTGG (MSH6)	ENSP00000397484.2:p.Ile159=
ENST00000700004.2:c.773_776delinsTTGG (MSH6)	ENSP00000514752.2:p.Ile258=
ENST00000699999.1:n.857_860delinsTTGG (MSH6)
ENST00000700000.1:c.773_776delinsTTGG (MSH6)	ENSP00000514749.1:p.Ile258=
ENST00000700002.1:c.779_782delinsTTGG (MSH6)	ENSP00000514750.1:p.Ile260=
ENST00000700003.1:c.627+2693_627+2696delinsTTGG (MSH6)	ENSP00000514751.1:n.627+2693_627+2696delinsTTGG
ENST00000234420.11:c.773_776delinsTTGG (MSH6) MANE Select	ENSP00000234420.5:p.Ile258=
ENST00000540021.6:c.383_386delinsTTGG (MSH6)	ENSP00000446475.1:p.Ile128=
ENST00000652107.1:c.476_479delinsTTGG (MSH6)	ENSP00000498629.1:p.Ile159=
ENST00000673637.1:c.476_479delinsTTGG (MSH6)	ENSP00000501310.1:p.Ile159=
ENST00000673922.1:n.495_498delinsTTGG (MSH6)
ENST00000234420.9:c.773_776delinsTTGG (MSH6)	ENSP00000234420.4:p.Ile258=
ENST00000405808.5:c.170-9319_170-9316delinsCCAA (FBXO11)	ENSP00000385127.1:n.170-9319_170-9316delinsCCAA
ENST00000434234.5:c.*124+9235_*124+9238delinsCCAA (FBXO11)	ENSP00000402692.1:n.*124+9235_*124+9238delinsCCAA
ENST00000445503.5:c.*120_*123delinsTTGG (MSH6)	ENSP00000405294.1:n.*120_*123delinsTTGG
ENST00000456246.1:c.*261_*264delinsTTGG (MSH6)	ENSP00000410570.1:n.*261_*264delinsTTGG
ENST00000538136.1:c.-134_-131delinsTTGG (MSH6)	ENSP00000438580.1:n.-134_-131delinsTTGG
ENST00000540021.5:c.383_386delinsTTGG (MSH6)	ENSP00000446475.1:p.Ile128=
ENST00000614496.4:c.-134_-131delinsTTGG (MSH6)	ENSP00000477844.1:n.-134_-131delinsTTGG
ENST00000616033.4:c.770_773delinsTTGG (MSH6)	ENSP00000480261.1:p.Ile257=
ENST00000622629.4:c.-2324_-2321delinsTTGG (MSH6)	ENSP00000482078.1:n.-2324_-2321delinsTTGG
NM_000179.2:c.773_776delinsTTGG , LRG_219t1:c.773_776delinsTTGG (MSH6)	NP_000170.1:p.Ile258=
NM_001281492.1:c.383_386delinsTTGG (MSH6)	NP_001268421.1:p.Ile128=
NM_001281493.1:c.-134_-131delinsTTGG (MSH6)	NP_001268422.1:n.-134_-131delinsTTGG
NM_001281494.1:c.-134_-131delinsTTGG (MSH6)	NP_001268423.1:n.-134_-131delinsTTGG
XM_005264271.1:c.476_479delinsTTGG (MSH6)	XP_005264328.1:p.Ile159=
XM_011532798.1:c.590_593delinsTTGG (MSH6)	XP_011531100.1:p.Ile197=
XM_011532799.1:c.476_479delinsTTGG (MSH6)	XP_011531101.1:p.Ile159=
XM_011532800.1:c.476_479delinsTTGG (MSH6)	XP_011531102.1:p.Ile159=
XM_024452819.1:c.773_776delinsTTGG (MSH6)	XP_024308587.1:p.Ile258=
XM_024452820.1:c.590_593delinsTTGG (MSH6)	XP_024308588.1:p.Ile197=
XM_024452821.1:c.476_479delinsTTGG (MSH6)	XP_024308589.1:p.Ile159=
XM_024452822.1:c.-134_-131delinsTTGG (MSH6)	XP_024308590.1:n.-134_-131delinsTTGG
NM_000179.3:c.773_776delinsTTGG (MSH6) MANE Select	NP_000170.1:p.Ile258=
NM_001281492.2:c.383_386delinsTTGG (MSH6)	NP_001268421.1:p.Ile128=
NM_001281493.2:c.-134_-131delinsTTGG (MSH6)	NP_001268422.1:n.-134_-131delinsTTGG
NM_001281494.2:c.-134_-131delinsTTGG (MSH6)	NP_001268423.1:n.-134_-131delinsTTGG