Canonical Allele Identifier: CA346761174

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1553333156
• MyVariant Identifiers: chr2:g.48033485C>A (hg19) ; chr2:g.47806346C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806346C>A , CM000664.2:g.47806346C>A	GRCh38
NC_000002.11:g.48033485C>A , CM000664.1:g.48033485C>A	GRCh37
NC_000002.10:g.47886989C>A	NCBI36
NG_007111.1:g.28200C>A , LRG_219:g.28200C>A
NG_008397.1:g.104330G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3492C>A (MSH6)	ENSP00000406248.2:p.Arg1164=
ENST00000420813.6:c.3492C>A (MSH6)	ENSP00000390382.2:p.Arg1164=
ENST00000455383.6:c.3492C>A (MSH6)	ENSP00000397484.2:p.Arg1164=
ENST00000700004.2:c.3405C>A (MSH6)	ENSP00000514752.2:p.Arg1135=
ENST00000699999.1:n.4463C>A (MSH6)
ENST00000700000.1:c.2223C>A (MSH6)	ENSP00000514749.1:p.Arg741=
ENST00000700002.1:c.3795C>A (MSH6)	ENSP00000514750.1:p.Arg1265=
ENST00000700003.1:c.1244C>A (MSH6)	ENSP00000514751.1:n.1244C>A
ENST00000700004.1:c.2562C>A (MSH6)	ENSP00000514752.1:p.Arg854=
ENST00000700005.1:n.2640C>A (MSH6)
ENST00000700006.1:n.4947C>A (MSH6)
ENST00000700007.1:n.2384C>A (MSH6)
ENST00000700008.1:n.1958C>A (MSH6)
ENST00000700009.1:n.2453C>A (MSH6)
ENST00000700010.1:n.1198C>A (MSH6)
ENST00000700011.1:n.3083C>A (MSH6)
ENST00000682451.1:n.4402G>T (FBXO11)
ENST00000684712.1:n.4664G>T (FBXO11)
ENST00000234420.11:c.3789C>A (MSH6) MANE Select	ENSP00000234420.5:p.Arg1263=
ENST00000540021.6:c.3399C>A (MSH6)	ENSP00000446475.1:p.Arg1133=
ENST00000652107.1:c.3492C>A (MSH6)	ENSP00000498629.1:p.Arg1164=
ENST00000673637.1:c.3492C>A (MSH6)	ENSP00000501310.1:p.Arg1164=
ENST00000234420.9:c.3789C>A (MSH6)	ENSP00000234420.4:p.Arg1263=
ENST00000405808.5:c.169+1849G>T (FBXO11)	ENSP00000385127.1:n.169+1849G>T
ENST00000434234.5:c.*124+1648G>T (FBXO11)	ENSP00000402692.1:n.*124+1648G>T
ENST00000445503.5:c.*3136C>A (MSH6)	ENSP00000405294.1:n.*3136C>A
ENST00000538136.1:c.2883C>A (MSH6)	ENSP00000438580.1:p.Arg961=
ENST00000540021.5:c.3399C>A (MSH6)	ENSP00000446475.1:p.Arg1133=
ENST00000614496.4:c.2883C>A (MSH6)	ENSP00000477844.1:p.Arg961=
ENST00000622629.4:c.691-1C>A (MSH6)	ENSP00000482078.1:n.691-1C>A
NM_000179.2:c.3789C>A , LRG_219t1:c.3789C>A (MSH6)	NP_000170.1:p.Arg1263=
NM_001281492.1:c.3399C>A (MSH6)	NP_001268421.1:p.Arg1133=
NM_001281493.1:c.2883C>A (MSH6)	NP_001268422.1:p.Arg961=
NM_001281494.1:c.2883C>A (MSH6)	NP_001268423.1:p.Arg961=
XM_005264271.1:c.3492C>A (MSH6)	XP_005264328.1:p.Arg1164=
XM_011532798.1:c.3606C>A (MSH6)	XP_011531100.1:p.Arg1202=
XM_011532799.1:c.3492C>A (MSH6)	XP_011531101.1:p.Arg1164=
XM_011532800.1:c.3492C>A (MSH6)	XP_011531102.1:p.Arg1164=
XM_024452819.1:c.3789C>A (MSH6)	XP_024308587.1:p.Arg1263=
XM_024452820.1:c.3606C>A (MSH6)	XP_024308588.1:p.Arg1202=
XM_024452821.1:c.3492C>A (MSH6)	XP_024308589.1:p.Arg1164=
XM_024452822.1:c.2883C>A (MSH6)	XP_024308590.1:p.Arg961=
NM_000179.3:c.3789C>A (MSH6) MANE Select	NP_000170.1:p.Arg1263=
NM_001281492.2:c.3399C>A (MSH6)	NP_001268421.1:p.Arg1133=
NM_001281493.2:c.2883C>A (MSH6)	NP_001268422.1:p.Arg961=
NM_001281494.2:c.2883C>A (MSH6)	NP_001268423.1:p.Arg961=