Canonical Allele Identifier: CA2496049909

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800855_47800856delinsCA , CM000664.2:g.47800855_47800856delinsCA	GRCh38
NC_000002.11:g.48027994_48027995delinsCA , CM000664.1:g.48027994_48027995delinsCA	GRCh37
NC_000002.10:g.47881498_47881499delinsCA	NCBI36
NG_007111.1:g.22709_22710delinsCA , LRG_219:g.22709_22710delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2575_2576delinsCA (MSH6)	ENSP00000406248.2:p.Gln859=
ENST00000420813.6:c.2575_2576delinsCA (MSH6)	ENSP00000390382.2:p.Gln859=
ENST00000455383.6:c.2575_2576delinsCA (MSH6)	ENSP00000397484.2:p.Gln859=
ENST00000700004.2:c.2872_2873delinsCA (MSH6)	ENSP00000514752.2:p.Gln958=
ENST00000699999.1:n.2956_2957delinsCA (MSH6)
ENST00000700000.1:c.1606+1266_1606+1267delinsCA (MSH6)	ENSP00000514749.1:n.1606+1266_1606+1267delinsCA
ENST00000700002.1:c.2878_2879delinsCA (MSH6)	ENSP00000514750.1:p.Gln960=
ENST00000700003.1:c.628-2565_628-2564delinsCA (MSH6)	ENSP00000514751.1:n.628-2565_628-2564delinsCA
ENST00000700004.1:c.2029_2030delinsCA (MSH6)	ENSP00000514752.1:p.Gln677=
ENST00000234420.11:c.2872_2873delinsCA (MSH6) MANE Select	ENSP00000234420.5:p.Gln958=
ENST00000540021.6:c.2482_2483delinsCA (MSH6)	ENSP00000446475.1:p.Gln828=
ENST00000652107.1:c.2575_2576delinsCA (MSH6)	ENSP00000498629.1:p.Gln859=
ENST00000673637.1:c.2575_2576delinsCA (MSH6)	ENSP00000501310.1:p.Gln859=
ENST00000234420.9:c.2872_2873delinsCA (MSH6)	ENSP00000234420.4:p.Gln958=
ENST00000405808.5:c.169+7339_169+7340delinsTG (FBXO11)	ENSP00000385127.1:n.169+7339_169+7340delinsTG
ENST00000434234.5:c.*124+7138_*124+7139delinsTG (FBXO11)	ENSP00000402692.1:n.*124+7138_*124+7139delinsTG
ENST00000445503.5:c.*2219_*2220delinsCA (MSH6)	ENSP00000405294.1:n.*2219_*2220delinsCA
ENST00000538136.1:c.1966_1967delinsCA (MSH6)	ENSP00000438580.1:p.Gln656=
ENST00000540021.5:c.2482_2483delinsCA (MSH6)	ENSP00000446475.1:p.Gln828=
ENST00000614496.4:c.1966_1967delinsCA (MSH6)	ENSP00000477844.1:p.Gln656=
ENST00000616033.4:c.2869_2870delinsCA (MSH6)	ENSP00000480261.1:p.Gln957=
ENST00000622629.4:c.-225_-224delinsCA (MSH6)	ENSP00000482078.1:n.-225_-224delinsCA
NM_000179.2:c.2872_2873delinsCA , LRG_219t1:c.2872_2873delinsCA (MSH6)	NP_000170.1:p.Gln958=
NM_001281492.1:c.2482_2483delinsCA (MSH6)	NP_001268421.1:p.Gln828=
NM_001281493.1:c.1966_1967delinsCA (MSH6)	NP_001268422.1:p.Gln656=
NM_001281494.1:c.1966_1967delinsCA (MSH6)	NP_001268423.1:p.Gln656=
XM_005264271.1:c.2575_2576delinsCA (MSH6)	XP_005264328.1:p.Gln859=
XM_011532798.1:c.2689_2690delinsCA (MSH6)	XP_011531100.1:p.Gln897=
XM_011532799.1:c.2575_2576delinsCA (MSH6)	XP_011531101.1:p.Gln859=
XM_011532800.1:c.2575_2576delinsCA (MSH6)	XP_011531102.1:p.Gln859=
XM_024452819.1:c.2872_2873delinsCA (MSH6)	XP_024308587.1:p.Gln958=
XM_024452820.1:c.2689_2690delinsCA (MSH6)	XP_024308588.1:p.Gln897=
XM_024452821.1:c.2575_2576delinsCA (MSH6)	XP_024308589.1:p.Gln859=
XM_024452822.1:c.1966_1967delinsCA (MSH6)	XP_024308590.1:p.Gln656=
NM_000179.3:c.2872_2873delinsCA (MSH6) MANE Select	NP_000170.1:p.Gln958=
NM_001281492.2:c.2482_2483delinsCA (MSH6)	NP_001268421.1:p.Gln828=
NM_001281493.2:c.1966_1967delinsCA (MSH6)	NP_001268422.1:p.Gln656=
NM_001281494.2:c.1966_1967delinsCA (MSH6)	NP_001268423.1:p.Gln656=