Canonical Allele Identifier: CA2496053821

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806055C= , CM000664.2:g.47806055C=	GRCh38
NC_000002.11:g.48033194C= , CM000664.1:g.48033194C=	GRCh37
NC_000002.10:g.47886698C=	NCBI36
NG_007111.1:g.27909C= , LRG_219:g.27909C=
NG_008397.1:g.104621G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3350-149C= (MSH6)	ENSP00000406248.2:n.3350-149C=
ENST00000420813.6:c.3350-149C= (MSH6)	ENSP00000390382.2:n.3350-149C=
ENST00000455383.6:c.3350-149C= (MSH6)	ENSP00000397484.2:n.3350-149C=
ENST00000700004.2:c.3263-149C= (MSH6)	ENSP00000514752.2:n.3263-149C=
ENST00000699999.1:n.4321-149C= (MSH6)
ENST00000700000.1:c.2081-149C= (MSH6)	ENSP00000514749.1:n.2081-149C=
ENST00000700002.1:c.3653-149C= (MSH6)	ENSP00000514750.1:n.3653-149C=
ENST00000700003.1:c.1102-149C= (MSH6)	ENSP00000514751.1:n.1102-149C=
ENST00000700004.1:c.2420-149C= (MSH6)	ENSP00000514752.1:n.2420-149C=
ENST00000700005.1:n.2498-149C= (MSH6)
ENST00000700006.1:n.4656C= (MSH6)
ENST00000700007.1:n.2242-149C= (MSH6)
ENST00000700008.1:n.1816-149C= (MSH6)
ENST00000700009.1:n.2162C= (MSH6)
ENST00000700010.1:n.1056-149C= (MSH6)
ENST00000700011.1:n.2941-149C= (MSH6)
ENST00000682451.1:n.4693G= (FBXO11)
ENST00000684712.1:n.4955G= (FBXO11)
ENST00000234420.11:c.3647-149C= (MSH6) MANE Select	ENSP00000234420.5:n.3647-149C=
ENST00000540021.6:c.3257-149C= (MSH6)	ENSP00000446475.1:n.3257-149C=
ENST00000652107.1:c.3350-149C= (MSH6)	ENSP00000498629.1:n.3350-149C=
ENST00000673637.1:c.3350-149C= (MSH6)	ENSP00000501310.1:n.3350-149C=
ENST00000234420.9:c.3647-149C= (MSH6)	ENSP00000234420.4:n.3647-149C=
ENST00000405808.5:c.169+2140G= (FBXO11)	ENSP00000385127.1:n.169+2140G=
ENST00000434234.5:c.*124+1939G= (FBXO11)	ENSP00000402692.1:n.*124+1939G=
ENST00000445503.5:c.*2994-149C= (MSH6)	ENSP00000405294.1:n.*2994-149C=
ENST00000538136.1:c.2741-149C= (MSH6)	ENSP00000438580.1:n.2741-149C=
ENST00000540021.5:c.3257-149C= (MSH6)	ENSP00000446475.1:n.3257-149C=
ENST00000614496.4:c.2741-149C= (MSH6)	ENSP00000477844.1:n.2741-149C=
ENST00000622629.4:c.551-149C= (MSH6)	ENSP00000482078.1:n.551-149C=
NM_000179.2:c.3647-149C= , LRG_219t1:c.3647-149C= (MSH6)	NP_000170.1:n.3647-149C=
NM_001281492.1:c.3257-149C= (MSH6)	NP_001268421.1:n.3257-149C=
NM_001281493.1:c.2741-149C= (MSH6)	NP_001268422.1:n.2741-149C=
NM_001281494.1:c.2741-149C= (MSH6)	NP_001268423.1:n.2741-149C=
XM_005264271.1:c.3350-149C= (MSH6)	XP_005264328.1:n.3350-149C=
XM_011532798.1:c.3464-149C= (MSH6)	XP_011531100.1:n.3464-149C=
XM_011532799.1:c.3350-149C= (MSH6)	XP_011531101.1:n.3350-149C=
XM_011532800.1:c.3350-149C= (MSH6)	XP_011531102.1:n.3350-149C=
XM_024452819.1:c.3647-149C= (MSH6)	XP_024308587.1:n.3647-149C=
XM_024452820.1:c.3464-149C= (MSH6)	XP_024308588.1:n.3464-149C=
XM_024452821.1:c.3350-149C= (MSH6)	XP_024308589.1:n.3350-149C=
XM_024452822.1:c.2741-149C= (MSH6)	XP_024308590.1:n.2741-149C=
NM_000179.3:c.3647-149C= (MSH6) MANE Select	NP_000170.1:n.3647-149C=
NM_001281492.2:c.3257-149C= (MSH6)	NP_001268421.1:n.3257-149C=
NM_001281493.2:c.2741-149C= (MSH6)	NP_001268422.1:n.2741-149C=
NM_001281494.2:c.2741-149C= (MSH6)	NP_001268423.1:n.2741-149C=