Canonical Allele Identifier: CA2496049518

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800452_47800453delinsTA , CM000664.2:g.47800452_47800453delinsTA	GRCh38
NC_000002.11:g.48027591_48027592delinsTA , CM000664.1:g.48027591_48027592delinsTA	GRCh37
NC_000002.10:g.47881095_47881096delinsTA	NCBI36
NG_007111.1:g.22306_22307delinsTA , LRG_219:g.22306_22307delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2172_2173delinsTA (MSH6)	ENSP00000406248.2:p.Ser724=
ENST00000420813.6:c.2172_2173delinsTA (MSH6)	ENSP00000390382.2:p.Ser724=
ENST00000455383.6:c.2172_2173delinsTA (MSH6)	ENSP00000397484.2:p.Ser724=
ENST00000700004.2:c.2469_2470delinsTA (MSH6)	ENSP00000514752.2:p.Ser823=
ENST00000699999.1:n.2553_2554delinsTA (MSH6)
ENST00000700000.1:c.1606+863_1606+864delinsTA (MSH6)	ENSP00000514749.1:n.1606+863_1606+864delinsTA
ENST00000700002.1:c.2475_2476delinsTA (MSH6)	ENSP00000514750.1:p.Ser825=
ENST00000700003.1:c.628-2968_628-2967delinsTA (MSH6)	ENSP00000514751.1:n.628-2968_628-2967delinsTA
ENST00000700004.1:c.1626_1627delinsTA (MSH6)	ENSP00000514752.1:p.Ser542=
ENST00000234420.11:c.2469_2470delinsTA (MSH6) MANE Select	ENSP00000234420.5:p.Ser823=
ENST00000540021.6:c.2079_2080delinsTA (MSH6)	ENSP00000446475.1:p.Ser693=
ENST00000652107.1:c.2172_2173delinsTA (MSH6)	ENSP00000498629.1:p.Ser724=
ENST00000673637.1:c.2172_2173delinsTA (MSH6)	ENSP00000501310.1:p.Ser724=
ENST00000234420.9:c.2469_2470delinsTA (MSH6)	ENSP00000234420.4:p.Ser823=
ENST00000405808.5:c.169+7742_169+7743delinsTA (FBXO11)	ENSP00000385127.1:n.169+7742_169+7743delinsTA
ENST00000434234.5:c.*124+7541_*124+7542delinsTA (FBXO11)	ENSP00000402692.1:n.*124+7541_*124+7542delinsTA
ENST00000445503.5:c.*1816_*1817delinsTA (MSH6)	ENSP00000405294.1:n.*1816_*1817delinsTA
ENST00000538136.1:c.1563_1564delinsTA (MSH6)	ENSP00000438580.1:p.Ser521=
ENST00000540021.5:c.2079_2080delinsTA (MSH6)	ENSP00000446475.1:p.Ser693=
ENST00000614496.4:c.1563_1564delinsTA (MSH6)	ENSP00000477844.1:p.Ser521=
ENST00000616033.4:c.2466_2467delinsTA (MSH6)	ENSP00000480261.1:p.Ser822=
ENST00000622629.4:c.-628_-627delinsTA (MSH6)	ENSP00000482078.1:n.-628_-627delinsTA
NM_000179.2:c.2469_2470delinsTA , LRG_219t1:c.2469_2470delinsTA (MSH6)	NP_000170.1:p.Ser823=
NM_001281492.1:c.2079_2080delinsTA (MSH6)	NP_001268421.1:p.Ser693=
NM_001281493.1:c.1563_1564delinsTA (MSH6)	NP_001268422.1:p.Ser521=
NM_001281494.1:c.1563_1564delinsTA (MSH6)	NP_001268423.1:p.Ser521=
XM_005264271.1:c.2172_2173delinsTA (MSH6)	XP_005264328.1:p.Ser724=
XM_011532798.1:c.2286_2287delinsTA (MSH6)	XP_011531100.1:p.Ser762=
XM_011532799.1:c.2172_2173delinsTA (MSH6)	XP_011531101.1:p.Ser724=
XM_011532800.1:c.2172_2173delinsTA (MSH6)	XP_011531102.1:p.Ser724=
XM_024452819.1:c.2469_2470delinsTA (MSH6)	XP_024308587.1:p.Ser823=
XM_024452820.1:c.2286_2287delinsTA (MSH6)	XP_024308588.1:p.Ser762=
XM_024452821.1:c.2172_2173delinsTA (MSH6)	XP_024308589.1:p.Ser724=
XM_024452822.1:c.1563_1564delinsTA (MSH6)	XP_024308590.1:p.Ser521=
NM_000179.3:c.2469_2470delinsTA (MSH6) MANE Select	NP_000170.1:p.Ser823=
NM_001281492.2:c.2079_2080delinsTA (MSH6)	NP_001268421.1:p.Ser693=
NM_001281493.2:c.1563_1564delinsTA (MSH6)	NP_001268422.1:p.Ser521=
NM_001281494.2:c.1563_1564delinsTA (MSH6)	NP_001268423.1:p.Ser521=