Canonical Allele Identifier: CA346745135

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 455134
• ClinVar RCV Id: RCV000537341 ; RCV000572517
• dbSNP Id: rs1553412811
• MyVariant Identifiers: chr2:g.48026516C>T (hg19) ; chr2:g.47799377C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799377C>T , CM000664.2:g.47799377C>T	GRCh38
NC_000002.11:g.48026516C>T , CM000664.1:g.48026516C>T	GRCh37
NC_000002.10:g.47880020C>T	NCBI36
NG_007111.1:g.21231C>T , LRG_219:g.21231C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.1097C>T (MSH6)	ENSP00000406248.2:p.Ala366Val
ENST00000420813.6:c.1097C>T (MSH6)	ENSP00000390382.2:p.Ala366Val
ENST00000455383.6:c.1097C>T (MSH6)	ENSP00000397484.2:p.Ala366Val
ENST00000700004.2:c.1394C>T (MSH6)	ENSP00000514752.2:p.Ala465Val
ENST00000699999.1:n.1478C>T (MSH6)
ENST00000700000.1:c.1394C>T (MSH6)	ENSP00000514749.1:p.Ala465Val
ENST00000700002.1:c.1400C>T (MSH6)	ENSP00000514750.1:p.Ala467Val
ENST00000700003.1:c.627+3314C>T (MSH6)	ENSP00000514751.1:n.627+3314C>T
ENST00000700004.1:c.551C>T (MSH6)	ENSP00000514752.1:p.Ala184Val
ENST00000234420.11:c.1394C>T (MSH6) MANE Select	ENSP00000234420.5:p.Ala465Val
ENST00000540021.6:c.1004C>T (MSH6)	ENSP00000446475.1:p.Ala335Val
ENST00000652107.1:c.1097C>T (MSH6)	ENSP00000498629.1:p.Ala366Val
ENST00000673637.1:c.1097C>T (MSH6)	ENSP00000501310.1:p.Ala366Val
ENST00000234420.9:c.1394C>T (MSH6)	ENSP00000234420.4:p.Ala465Val
ENST00000405808.5:c.169+8818G>A (FBXO11)	ENSP00000385127.1:n.169+8818G>A
ENST00000434234.5:c.*124+8617G>A (FBXO11)	ENSP00000402692.1:n.*124+8617G>A
ENST00000445503.5:c.*741C>T (MSH6)	ENSP00000405294.1:n.*741C>T
ENST00000538136.1:c.488C>T (MSH6)	ENSP00000438580.1:p.Ala163Val
ENST00000540021.5:c.1004C>T (MSH6)	ENSP00000446475.1:p.Ala335Val
ENST00000614496.4:c.488C>T (MSH6)	ENSP00000477844.1:p.Ala163Val
ENST00000616033.4:c.1391C>T (MSH6)	ENSP00000480261.1:p.Ala464Val
ENST00000622629.4:c.-1703C>T (MSH6)	ENSP00000482078.1:n.-1703C>T
NM_000179.2:c.1394C>T , LRG_219t1:c.1394C>T (MSH6)	NP_000170.1:p.Ala465Val
NM_001281492.1:c.1004C>T (MSH6)	NP_001268421.1:p.Ala335Val
NM_001281493.1:c.488C>T (MSH6)	NP_001268422.1:p.Ala163Val
NM_001281494.1:c.488C>T (MSH6)	NP_001268423.1:p.Ala163Val
XM_005264271.1:c.1097C>T (MSH6)	XP_005264328.1:p.Ala366Val
XM_011532798.1:c.1211C>T (MSH6)	XP_011531100.1:p.Ala404Val
XM_011532799.1:c.1097C>T (MSH6)	XP_011531101.1:p.Ala366Val
XM_011532800.1:c.1097C>T (MSH6)	XP_011531102.1:p.Ala366Val
XM_024452819.1:c.1394C>T (MSH6)	XP_024308587.1:p.Ala465Val
XM_024452820.1:c.1211C>T (MSH6)	XP_024308588.1:p.Ala404Val
XM_024452821.1:c.1097C>T (MSH6)	XP_024308589.1:p.Ala366Val
XM_024452822.1:c.488C>T (MSH6)	XP_024308590.1:p.Ala163Val
NM_000179.3:c.1394C>T (MSH6) MANE Select	NP_000170.1:p.Ala465Val
NM_001281492.2:c.1004C>T (MSH6)	NP_001268421.1:p.Ala335Val
NM_001281493.2:c.488C>T (MSH6)	NP_001268422.1:p.Ala163Val
NM_001281494.2:c.488C>T (MSH6)	NP_001268423.1:p.Ala163Val