Canonical Allele Identifier: CA2496048373

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799039_47799044delinsTAGTGG , CM000664.2:g.47799039_47799044delinsTAGTGG	GRCh38
NC_000002.11:g.48026178_48026183delinsTAGTGG , CM000664.1:g.48026178_48026183delinsTAGTGG	GRCh37
NC_000002.10:g.47879682_47879687delinsTAGTGG	NCBI36
NG_007111.1:g.20893_20898delinsTAGTGG , LRG_219:g.20893_20898delinsTAGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.759_764delinsTAGTGG (MSH6)	ENSP00000406248.2:p.Val253=
ENST00000420813.6:c.759_764delinsTAGTGG (MSH6)	ENSP00000390382.2:p.Val253=
ENST00000455383.6:c.759_764delinsTAGTGG (MSH6)	ENSP00000397484.2:p.Val253=
ENST00000700004.2:c.1056_1061delinsTAGTGG (MSH6)	ENSP00000514752.2:p.Val352=
ENST00000699999.1:n.1140_1145delinsTAGTGG (MSH6)
ENST00000700000.1:c.1056_1061delinsTAGTGG (MSH6)	ENSP00000514749.1:p.Val352=
ENST00000700002.1:c.1062_1067delinsTAGTGG (MSH6)	ENSP00000514750.1:p.Val354=
ENST00000700003.1:c.627+2976_627+2981delinsTAGTGG (MSH6)	ENSP00000514751.1:n.627+2976_627+2981delinsTAGTGG
ENST00000700004.1:c.213_218delinsTAGTGG (MSH6)	ENSP00000514752.1:p.Val71=
ENST00000234420.11:c.1056_1061delinsTAGTGG (MSH6) MANE Select	ENSP00000234420.5:p.Val352=
ENST00000540021.6:c.666_671delinsTAGTGG (MSH6)	ENSP00000446475.1:p.Val222=
ENST00000652107.1:c.759_764delinsTAGTGG (MSH6)	ENSP00000498629.1:p.Val253=
ENST00000673637.1:c.759_764delinsTAGTGG (MSH6)	ENSP00000501310.1:p.Val253=
ENST00000234420.9:c.1056_1061delinsTAGTGG (MSH6)	ENSP00000234420.4:p.Val352=
ENST00000405808.5:c.169+9151_169+9156delinsCCACTA (FBXO11)	ENSP00000385127.1:n.169+9151_169+9156delinsCCACTA
ENST00000434234.5:c.*124+8950_*124+8955delinsCCACTA (FBXO11)	ENSP00000402692.1:n.*124+8950_*124+8955delinsCCACTA
ENST00000445503.5:c.*403_*408delinsTAGTGG (MSH6)	ENSP00000405294.1:n.*403_*408delinsTAGTGG
ENST00000538136.1:c.150_155delinsTAGTGG (MSH6)	ENSP00000438580.1:p.Val50=
ENST00000540021.5:c.666_671delinsTAGTGG (MSH6)	ENSP00000446475.1:p.Val222=
ENST00000614496.4:c.150_155delinsTAGTGG (MSH6)	ENSP00000477844.1:p.Val50=
ENST00000616033.4:c.1053_1058delinsTAGTGG (MSH6)	ENSP00000480261.1:p.Val351=
ENST00000622629.4:c.-2041_-2036delinsTAGTGG (MSH6)	ENSP00000482078.1:n.-2041_-2036delinsTAGTGG
NM_000179.2:c.1056_1061delinsTAGTGG , LRG_219t1:c.1056_1061delinsTAGTGG (MSH6)	NP_000170.1:p.Val352=
NM_001281492.1:c.666_671delinsTAGTGG (MSH6)	NP_001268421.1:p.Val222=
NM_001281493.1:c.150_155delinsTAGTGG (MSH6)	NP_001268422.1:p.Val50=
NM_001281494.1:c.150_155delinsTAGTGG (MSH6)	NP_001268423.1:p.Val50=
XM_005264271.1:c.759_764delinsTAGTGG (MSH6)	XP_005264328.1:p.Val253=
XM_011532798.1:c.873_878delinsTAGTGG (MSH6)	XP_011531100.1:p.Val291=
XM_011532799.1:c.759_764delinsTAGTGG (MSH6)	XP_011531101.1:p.Val253=
XM_011532800.1:c.759_764delinsTAGTGG (MSH6)	XP_011531102.1:p.Val253=
XM_024452819.1:c.1056_1061delinsTAGTGG (MSH6)	XP_024308587.1:p.Val352=
XM_024452820.1:c.873_878delinsTAGTGG (MSH6)	XP_024308588.1:p.Val291=
XM_024452821.1:c.759_764delinsTAGTGG (MSH6)	XP_024308589.1:p.Val253=
XM_024452822.1:c.150_155delinsTAGTGG (MSH6)	XP_024308590.1:p.Val50=
NM_000179.3:c.1056_1061delinsTAGTGG (MSH6) MANE Select	NP_000170.1:p.Val352=
NM_001281492.2:c.666_671delinsTAGTGG (MSH6)	NP_001268421.1:p.Val222=
NM_001281493.2:c.150_155delinsTAGTGG (MSH6)	NP_001268422.1:p.Val50=
NM_001281494.2:c.150_155delinsTAGTGG (MSH6)	NP_001268423.1:p.Val50=