Canonical Allele Identifier: CA2496048103

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798717_47798721delinsTAAAA , CM000664.2:g.47798717_47798721delinsTAAAA	GRCh38
NC_000002.11:g.48025856_48025860delinsTAAAA , CM000664.1:g.48025856_48025860delinsTAAAA	GRCh37
NC_000002.10:g.47879360_47879364delinsTAAAA	NCBI36
NG_007111.1:g.20571_20575delinsTAAAA , LRG_219:g.20571_20575delinsTAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.437_441delinsTAAAA (MSH6)	ENSP00000406248.2:p.Ile146=
ENST00000420813.6:c.437_441delinsTAAAA (MSH6)	ENSP00000390382.2:p.Ile146=
ENST00000455383.6:c.437_441delinsTAAAA (MSH6)	ENSP00000397484.2:p.Ile146=
ENST00000700004.2:c.734_738delinsTAAAA (MSH6)	ENSP00000514752.2:p.Ile245=
ENST00000699999.1:n.818_822delinsTAAAA (MSH6)
ENST00000700000.1:c.734_738delinsTAAAA (MSH6)	ENSP00000514749.1:p.Ile245=
ENST00000700002.1:c.740_744delinsTAAAA (MSH6)	ENSP00000514750.1:p.Ile247=
ENST00000700003.1:c.627+2654_627+2658delinsTAAAA (MSH6)	ENSP00000514751.1:n.627+2654_627+2658delinsTAAAA
ENST00000234420.11:c.734_738delinsTAAAA (MSH6) MANE Select	ENSP00000234420.5:p.Ile245=
ENST00000540021.6:c.344_348delinsTAAAA (MSH6)	ENSP00000446475.1:p.Ile115=
ENST00000652107.1:c.437_441delinsTAAAA (MSH6)	ENSP00000498629.1:p.Ile146=
ENST00000673637.1:c.437_441delinsTAAAA (MSH6)	ENSP00000501310.1:p.Ile146=
ENST00000673922.1:n.456_460delinsTAAAA (MSH6)
ENST00000234420.9:c.734_738delinsTAAAA (MSH6)	ENSP00000234420.4:p.Ile245=
ENST00000405808.5:c.170-9281_170-9277delinsTTTTA (FBXO11)	ENSP00000385127.1:n.170-9281_170-9277delinsTTTTA
ENST00000411819.1:c.437_441delinsTAAAA (MSH6)	ENSP00000406248.1:p.Ile146=
ENST00000434234.5:c.*124+9273_*125-9277delinsTTTTA (FBXO11)	ENSP00000402692.1:n.*124+9273_*125-9277delinsTTTTA
ENST00000445503.5:c.*81_*85delinsTAAAA (MSH6)	ENSP00000405294.1:n.*81_*85delinsTAAAA
ENST00000456246.1:c.*222_*226delinsTAAAA (MSH6)	ENSP00000410570.1:n.*222_*226delinsTAAAA
ENST00000538136.1:c.-173_-169delinsTAAAA (MSH6)	ENSP00000438580.1:n.-173_-169delinsTAAAA
ENST00000540021.5:c.344_348delinsTAAAA (MSH6)	ENSP00000446475.1:p.Ile115=
ENST00000614496.4:c.-173_-169delinsTAAAA (MSH6)	ENSP00000477844.1:n.-173_-169delinsTAAAA
ENST00000616033.4:c.731_735delinsTAAAA (MSH6)	ENSP00000480261.1:p.Ile244=
ENST00000622629.4:c.-2363_-2359delinsTAAAA (MSH6)	ENSP00000482078.1:n.-2363_-2359delinsTAAAA
NM_000179.2:c.734_738delinsTAAAA , LRG_219t1:c.734_738delinsTAAAA (MSH6)	NP_000170.1:p.Ile245=
NM_001281492.1:c.344_348delinsTAAAA (MSH6)	NP_001268421.1:p.Ile115=
NM_001281493.1:c.-173_-169delinsTAAAA (MSH6)	NP_001268422.1:n.-173_-169delinsTAAAA
NM_001281494.1:c.-173_-169delinsTAAAA (MSH6)	NP_001268423.1:n.-173_-169delinsTAAAA
XM_005264271.1:c.437_441delinsTAAAA (MSH6)	XP_005264328.1:p.Ile146=
XM_011532798.1:c.551_555delinsTAAAA (MSH6)	XP_011531100.1:p.Ile184=
XM_011532799.1:c.437_441delinsTAAAA (MSH6)	XP_011531101.1:p.Ile146=
XM_011532800.1:c.437_441delinsTAAAA (MSH6)	XP_011531102.1:p.Ile146=
XM_024452819.1:c.734_738delinsTAAAA (MSH6)	XP_024308587.1:p.Ile245=
XM_024452820.1:c.551_555delinsTAAAA (MSH6)	XP_024308588.1:p.Ile184=
XM_024452821.1:c.437_441delinsTAAAA (MSH6)	XP_024308589.1:p.Ile146=
XM_024452822.1:c.-173_-169delinsTAAAA (MSH6)	XP_024308590.1:n.-173_-169delinsTAAAA
NM_000179.3:c.734_738delinsTAAAA (MSH6) MANE Select	NP_000170.1:p.Ile245=
NM_001281492.2:c.344_348delinsTAAAA (MSH6)	NP_001268421.1:p.Ile115=
NM_001281493.2:c.-173_-169delinsTAAAA (MSH6)	NP_001268422.1:n.-173_-169delinsTAAAA
NM_001281494.2:c.-173_-169delinsTAAAA (MSH6)	NP_001268423.1:n.-173_-169delinsTAAAA