Canonical Allele Identifier: CA346760868

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48033369A>C (hg19) ; chr2:g.47806230A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806230A>C , CM000664.2:g.47806230A>C	GRCh38
NC_000002.11:g.48033369A>C , CM000664.1:g.48033369A>C	GRCh37
NC_000002.10:g.47886873A>C	NCBI36
NG_007111.1:g.28084A>C , LRG_219:g.28084A>C
NG_008397.1:g.104446T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3376A>C (MSH6)	ENSP00000406248.2:p.Thr1126Pro
ENST00000420813.6:c.3376A>C (MSH6)	ENSP00000390382.2:p.Thr1126Pro
ENST00000455383.6:c.3376A>C (MSH6)	ENSP00000397484.2:p.Thr1126Pro
ENST00000700004.2:c.3289A>C (MSH6)	ENSP00000514752.2:p.Thr1097Pro
ENST00000699999.1:n.4347A>C (MSH6)
ENST00000700000.1:c.2107A>C (MSH6)	ENSP00000514749.1:p.Thr703Pro
ENST00000700002.1:c.3679A>C (MSH6)	ENSP00000514750.1:p.Thr1227Pro
ENST00000700003.1:c.1128A>C (MSH6)	ENSP00000514751.1:n.1128A>C
ENST00000700004.1:c.2446A>C (MSH6)	ENSP00000514752.1:p.Thr816Pro
ENST00000700005.1:n.2524A>C (MSH6)
ENST00000700006.1:n.4831A>C (MSH6)
ENST00000700007.1:n.2268A>C (MSH6)
ENST00000700008.1:n.1842A>C (MSH6)
ENST00000700009.1:n.2337A>C (MSH6)
ENST00000700010.1:n.1082A>C (MSH6)
ENST00000700011.1:n.2967A>C (MSH6)
ENST00000682451.1:n.4518T>G (FBXO11)
ENST00000684712.1:n.4780T>G (FBXO11)
ENST00000234420.11:c.3673A>C (MSH6) MANE Select	ENSP00000234420.5:p.Thr1225Pro
ENST00000540021.6:c.3283A>C (MSH6)	ENSP00000446475.1:p.Thr1095Pro
ENST00000652107.1:c.3376A>C (MSH6)	ENSP00000498629.1:p.Thr1126Pro
ENST00000673637.1:c.3376A>C (MSH6)	ENSP00000501310.1:p.Thr1126Pro
ENST00000234420.9:c.3673A>C (MSH6)	ENSP00000234420.4:p.Thr1225Pro
ENST00000405808.5:c.169+1965T>G (FBXO11)	ENSP00000385127.1:n.169+1965T>G
ENST00000434234.5:c.*124+1764T>G (FBXO11)	ENSP00000402692.1:n.*124+1764T>G
ENST00000445503.5:c.*3020A>C (MSH6)	ENSP00000405294.1:n.*3020A>C
ENST00000538136.1:c.2767A>C (MSH6)	ENSP00000438580.1:p.Thr923Pro
ENST00000540021.5:c.3283A>C (MSH6)	ENSP00000446475.1:p.Thr1095Pro
ENST00000614496.4:c.2767A>C (MSH6)	ENSP00000477844.1:p.Thr923Pro
ENST00000622629.4:c.577A>C (MSH6)	ENSP00000482078.1:p.Thr193Pro
NM_000179.2:c.3673A>C , LRG_219t1:c.3673A>C (MSH6)	NP_000170.1:p.Thr1225Pro
NM_001281492.1:c.3283A>C (MSH6)	NP_001268421.1:p.Thr1095Pro
NM_001281493.1:c.2767A>C (MSH6)	NP_001268422.1:p.Thr923Pro
NM_001281494.1:c.2767A>C (MSH6)	NP_001268423.1:p.Thr923Pro
XM_005264271.1:c.3376A>C (MSH6)	XP_005264328.1:p.Thr1126Pro
XM_011532798.1:c.3490A>C (MSH6)	XP_011531100.1:p.Thr1164Pro
XM_011532799.1:c.3376A>C (MSH6)	XP_011531101.1:p.Thr1126Pro
XM_011532800.1:c.3376A>C (MSH6)	XP_011531102.1:p.Thr1126Pro
XM_024452819.1:c.3673A>C (MSH6)	XP_024308587.1:p.Thr1225Pro
XM_024452820.1:c.3490A>C (MSH6)	XP_024308588.1:p.Thr1164Pro
XM_024452821.1:c.3376A>C (MSH6)	XP_024308589.1:p.Thr1126Pro
XM_024452822.1:c.2767A>C (MSH6)	XP_024308590.1:p.Thr923Pro
NM_000179.3:c.3673A>C (MSH6) MANE Select	NP_000170.1:p.Thr1225Pro
NM_001281492.2:c.3283A>C (MSH6)	NP_001268421.1:p.Thr1095Pro
NM_001281493.2:c.2767A>C (MSH6)	NP_001268422.1:p.Thr923Pro
NM_001281494.2:c.2767A>C (MSH6)	NP_001268423.1:p.Thr923Pro