Canonical Allele Identifier: CA2496048165

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798791_47798794delinsAAGG , CM000664.2:g.47798791_47798794delinsAAGG	GRCh38
NC_000002.11:g.48025930_48025933delinsAAGG , CM000664.1:g.48025930_48025933delinsAAGG	GRCh37
NC_000002.10:g.47879434_47879437delinsAAGG	NCBI36
NG_007111.1:g.20645_20648delinsAAGG , LRG_219:g.20645_20648delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.511_514delinsAAGG (MSH6)	ENSP00000406248.2:p.Lys171=
ENST00000420813.6:c.511_514delinsAAGG (MSH6)	ENSP00000390382.2:p.Lys171=
ENST00000455383.6:c.511_514delinsAAGG (MSH6)	ENSP00000397484.2:p.Lys171=
ENST00000700004.2:c.808_811delinsAAGG (MSH6)	ENSP00000514752.2:p.Lys270=
ENST00000699999.1:n.892_895delinsAAGG (MSH6)
ENST00000700000.1:c.808_811delinsAAGG (MSH6)	ENSP00000514749.1:p.Lys270=
ENST00000700002.1:c.814_817delinsAAGG (MSH6)	ENSP00000514750.1:p.Lys272=
ENST00000700003.1:c.627+2728_627+2731delinsAAGG (MSH6)	ENSP00000514751.1:n.627+2728_627+2731delinsAAGG
ENST00000234420.11:c.808_811delinsAAGG (MSH6) MANE Select	ENSP00000234420.5:p.Lys270=
ENST00000540021.6:c.418_421delinsAAGG (MSH6)	ENSP00000446475.1:p.Lys140=
ENST00000652107.1:c.511_514delinsAAGG (MSH6)	ENSP00000498629.1:p.Lys171=
ENST00000673637.1:c.511_514delinsAAGG (MSH6)	ENSP00000501310.1:p.Lys171=
ENST00000673922.1:n.530_533delinsAAGG (MSH6)
ENST00000234420.9:c.808_811delinsAAGG (MSH6)	ENSP00000234420.4:p.Lys270=
ENST00000405808.5:c.170-9354_170-9351delinsCCTT (FBXO11)	ENSP00000385127.1:n.170-9354_170-9351delinsCCTT
ENST00000434234.5:c.*124+9200_*124+9203delinsCCTT (FBXO11)	ENSP00000402692.1:n.*124+9200_*124+9203delinsCCTT
ENST00000445503.5:c.*155_*158delinsAAGG (MSH6)	ENSP00000405294.1:n.*155_*158delinsAAGG
ENST00000456246.1:c.*296_*299delinsAAGG (MSH6)	ENSP00000410570.1:n.*296_*299delinsAAGG
ENST00000538136.1:c.-99_-96delinsAAGG (MSH6)	ENSP00000438580.1:n.-99_-96delinsAAGG
ENST00000540021.5:c.418_421delinsAAGG (MSH6)	ENSP00000446475.1:p.Lys140=
ENST00000614496.4:c.-99_-96delinsAAGG (MSH6)	ENSP00000477844.1:n.-99_-96delinsAAGG
ENST00000616033.4:c.805_808delinsAAGG (MSH6)	ENSP00000480261.1:p.Lys269=
ENST00000622629.4:c.-2289_-2286delinsAAGG (MSH6)	ENSP00000482078.1:n.-2289_-2286delinsAAGG
NM_000179.2:c.808_811delinsAAGG , LRG_219t1:c.808_811delinsAAGG (MSH6)	NP_000170.1:p.Lys270=
NM_001281492.1:c.418_421delinsAAGG (MSH6)	NP_001268421.1:p.Lys140=
NM_001281493.1:c.-99_-96delinsAAGG (MSH6)	NP_001268422.1:n.-99_-96delinsAAGG
NM_001281494.1:c.-99_-96delinsAAGG (MSH6)	NP_001268423.1:n.-99_-96delinsAAGG
XM_005264271.1:c.511_514delinsAAGG (MSH6)	XP_005264328.1:p.Lys171=
XM_011532798.1:c.625_628delinsAAGG (MSH6)	XP_011531100.1:p.Lys209=
XM_011532799.1:c.511_514delinsAAGG (MSH6)	XP_011531101.1:p.Lys171=
XM_011532800.1:c.511_514delinsAAGG (MSH6)	XP_011531102.1:p.Lys171=
XM_024452819.1:c.808_811delinsAAGG (MSH6)	XP_024308587.1:p.Lys270=
XM_024452820.1:c.625_628delinsAAGG (MSH6)	XP_024308588.1:p.Lys209=
XM_024452821.1:c.511_514delinsAAGG (MSH6)	XP_024308589.1:p.Lys171=
XM_024452822.1:c.-99_-96delinsAAGG (MSH6)	XP_024308590.1:n.-99_-96delinsAAGG
NM_000179.3:c.808_811delinsAAGG (MSH6) MANE Select	NP_000170.1:p.Lys270=
NM_001281492.2:c.418_421delinsAAGG (MSH6)	NP_001268421.1:p.Lys140=
NM_001281493.2:c.-99_-96delinsAAGG (MSH6)	NP_001268422.1:n.-99_-96delinsAAGG
NM_001281494.2:c.-99_-96delinsAAGG (MSH6)	NP_001268423.1:n.-99_-96delinsAAGG