Canonical Allele Identifier: CA2496049910

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800855_47800857delinsCAG , CM000664.2:g.47800855_47800857delinsCAG	GRCh38
NC_000002.11:g.48027994_48027996delinsCAG , CM000664.1:g.48027994_48027996delinsCAG	GRCh37
NC_000002.10:g.47881498_47881500delinsCAG	NCBI36
NG_007111.1:g.22709_22711delinsCAG , LRG_219:g.22709_22711delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2575_2577delinsCAG (MSH6)	ENSP00000406248.2:p.Gln859=
ENST00000420813.6:c.2575_2577delinsCAG (MSH6)	ENSP00000390382.2:p.Gln859=
ENST00000455383.6:c.2575_2577delinsCAG (MSH6)	ENSP00000397484.2:p.Gln859=
ENST00000700004.2:c.2872_2874delinsCAG (MSH6)	ENSP00000514752.2:p.Gln958=
ENST00000699999.1:n.2956_2958delinsCAG (MSH6)
ENST00000700000.1:c.1606+1266_1606+1268delinsCAG (MSH6)	ENSP00000514749.1:n.1606+1266_1606+1268delinsCAG
ENST00000700002.1:c.2878_2880delinsCAG (MSH6)	ENSP00000514750.1:p.Gln960=
ENST00000700003.1:c.628-2565_628-2563delinsCAG (MSH6)	ENSP00000514751.1:n.628-2565_628-2563delinsCAG
ENST00000700004.1:c.2029_2031delinsCAG (MSH6)	ENSP00000514752.1:p.Gln677=
ENST00000234420.11:c.2872_2874delinsCAG (MSH6) MANE Select	ENSP00000234420.5:p.Gln958=
ENST00000540021.6:c.2482_2484delinsCAG (MSH6)	ENSP00000446475.1:p.Gln828=
ENST00000652107.1:c.2575_2577delinsCAG (MSH6)	ENSP00000498629.1:p.Gln859=
ENST00000673637.1:c.2575_2577delinsCAG (MSH6)	ENSP00000501310.1:p.Gln859=
ENST00000234420.9:c.2872_2874delinsCAG (MSH6)	ENSP00000234420.4:p.Gln958=
ENST00000405808.5:c.169+7338_169+7340delinsCTG (FBXO11)	ENSP00000385127.1:n.169+7338_169+7340delinsCTG
ENST00000434234.5:c.*124+7137_*124+7139delinsCTG (FBXO11)	ENSP00000402692.1:n.*124+7137_*124+7139delinsCTG
ENST00000445503.5:c.*2219_*2221delinsCAG (MSH6)	ENSP00000405294.1:n.*2219_*2221delinsCAG
ENST00000538136.1:c.1966_1968delinsCAG (MSH6)	ENSP00000438580.1:p.Gln656=
ENST00000540021.5:c.2482_2484delinsCAG (MSH6)	ENSP00000446475.1:p.Gln828=
ENST00000614496.4:c.1966_1968delinsCAG (MSH6)	ENSP00000477844.1:p.Gln656=
ENST00000616033.4:c.2869_2871delinsCAG (MSH6)	ENSP00000480261.1:p.Gln957=
ENST00000622629.4:c.-225_-223delinsCAG (MSH6)	ENSP00000482078.1:n.-225_-223delinsCAG
NM_000179.2:c.2872_2874delinsCAG , LRG_219t1:c.2872_2874delinsCAG (MSH6)	NP_000170.1:p.Gln958=
NM_001281492.1:c.2482_2484delinsCAG (MSH6)	NP_001268421.1:p.Gln828=
NM_001281493.1:c.1966_1968delinsCAG (MSH6)	NP_001268422.1:p.Gln656=
NM_001281494.1:c.1966_1968delinsCAG (MSH6)	NP_001268423.1:p.Gln656=
XM_005264271.1:c.2575_2577delinsCAG (MSH6)	XP_005264328.1:p.Gln859=
XM_011532798.1:c.2689_2691delinsCAG (MSH6)	XP_011531100.1:p.Gln897=
XM_011532799.1:c.2575_2577delinsCAG (MSH6)	XP_011531101.1:p.Gln859=
XM_011532800.1:c.2575_2577delinsCAG (MSH6)	XP_011531102.1:p.Gln859=
XM_024452819.1:c.2872_2874delinsCAG (MSH6)	XP_024308587.1:p.Gln958=
XM_024452820.1:c.2689_2691delinsCAG (MSH6)	XP_024308588.1:p.Gln897=
XM_024452821.1:c.2575_2577delinsCAG (MSH6)	XP_024308589.1:p.Gln859=
XM_024452822.1:c.1966_1968delinsCAG (MSH6)	XP_024308590.1:p.Gln656=
NM_000179.3:c.2872_2874delinsCAG (MSH6) MANE Select	NP_000170.1:p.Gln958=
NM_001281492.2:c.2482_2484delinsCAG (MSH6)	NP_001268421.1:p.Gln828=
NM_001281493.2:c.1966_1968delinsCAG (MSH6)	NP_001268422.1:p.Gln656=
NM_001281494.2:c.1966_1968delinsCAG (MSH6)	NP_001268423.1:p.Gln656=