Canonical Allele Identifier: CA2496049004

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799793G= , CM000664.2:g.47799793G=	GRCh38
NC_000002.11:g.48026932G= , CM000664.1:g.48026932G=	GRCh37
NC_000002.10:g.47880436G=	NCBI36
NG_007111.1:g.21647G= , LRG_219:g.21647G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.1513G= (MSH6)	ENSP00000406248.2:p.Glu505=
ENST00000420813.6:c.1513G= (MSH6)	ENSP00000390382.2:p.Glu505=
ENST00000455383.6:c.1513G= (MSH6)	ENSP00000397484.2:p.Glu505=
ENST00000700004.2:c.1810G= (MSH6)	ENSP00000514752.2:p.Glu604=
ENST00000699999.1:n.1894G= (MSH6)
ENST00000700000.1:c.1606+204G= (MSH6)	ENSP00000514749.1:n.1606+204G=
ENST00000700002.1:c.1816G= (MSH6)	ENSP00000514750.1:p.Glu606=
ENST00000700003.1:c.628-3627G= (MSH6)	ENSP00000514751.1:n.628-3627G=
ENST00000700004.1:c.967G= (MSH6)	ENSP00000514752.1:p.Glu323=
ENST00000234420.11:c.1810G= (MSH6) MANE Select	ENSP00000234420.5:p.Glu604=
ENST00000540021.6:c.1420G= (MSH6)	ENSP00000446475.1:p.Glu474=
ENST00000652107.1:c.1513G= (MSH6)	ENSP00000498629.1:p.Glu505=
ENST00000673637.1:c.1513G= (MSH6)	ENSP00000501310.1:p.Glu505=
ENST00000234420.9:c.1810G= (MSH6)	ENSP00000234420.4:p.Glu604=
ENST00000405808.5:c.169+8402C= (FBXO11)	ENSP00000385127.1:n.169+8402C=
ENST00000434234.5:c.*124+8201C= (FBXO11)	ENSP00000402692.1:n.*124+8201C=
ENST00000445503.5:c.*1157G= (MSH6)	ENSP00000405294.1:n.*1157G=
ENST00000538136.1:c.904G= (MSH6)	ENSP00000438580.1:p.Glu302=
ENST00000540021.5:c.1420G= (MSH6)	ENSP00000446475.1:p.Glu474=
ENST00000614496.4:c.904G= (MSH6)	ENSP00000477844.1:p.Glu302=
ENST00000616033.4:c.1807G= (MSH6)	ENSP00000480261.1:p.Glu603=
ENST00000622629.4:c.-1287G= (MSH6)	ENSP00000482078.1:n.-1287G=
NM_000179.2:c.1810G= , LRG_219t1:c.1810G= (MSH6)	NP_000170.1:p.Glu604=
NM_001281492.1:c.1420G= (MSH6)	NP_001268421.1:p.Glu474=
NM_001281493.1:c.904G= (MSH6)	NP_001268422.1:p.Glu302=
NM_001281494.1:c.904G= (MSH6)	NP_001268423.1:p.Glu302=
XM_005264271.1:c.1513G= (MSH6)	XP_005264328.1:p.Glu505=
XM_011532798.1:c.1627G= (MSH6)	XP_011531100.1:p.Glu543=
XM_011532799.1:c.1513G= (MSH6)	XP_011531101.1:p.Glu505=
XM_011532800.1:c.1513G= (MSH6)	XP_011531102.1:p.Glu505=
XM_024452819.1:c.1810G= (MSH6)	XP_024308587.1:p.Glu604=
XM_024452820.1:c.1627G= (MSH6)	XP_024308588.1:p.Glu543=
XM_024452821.1:c.1513G= (MSH6)	XP_024308589.1:p.Glu505=
XM_024452822.1:c.904G= (MSH6)	XP_024308590.1:p.Glu302=
NM_000179.3:c.1810G= (MSH6) MANE Select	NP_000170.1:p.Glu604=
NM_001281492.2:c.1420G= (MSH6)	NP_001268421.1:p.Glu474=
NM_001281493.2:c.904G= (MSH6)	NP_001268422.1:p.Glu302=
NM_001281494.2:c.904G= (MSH6)	NP_001268423.1:p.Glu302=