Canonical Allele Identifier: CA346740973

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 455361
• ClinVar RCV Id: RCV000546692 ; RCV002384034
• dbSNP Id: rs1553412397
• gnomAD v4: 2-47798956-C-T
• MyVariant Identifiers: chr2:g.48026095C>T (hg19) ; chr2:g.47798956C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798956C>T , CM000664.2:g.47798956C>T	GRCh38
NC_000002.11:g.48026095C>T , CM000664.1:g.48026095C>T	GRCh37
NC_000002.10:g.47879599C>T	NCBI36
NG_007111.1:g.20810C>T , LRG_219:g.20810C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.676C>T (MSH6)	ENSP00000406248.2:p.Gln226Ter
ENST00000420813.6:c.676C>T (MSH6)	ENSP00000390382.2:p.Gln226Ter
ENST00000455383.6:c.676C>T (MSH6)	ENSP00000397484.2:p.Gln226Ter
ENST00000700004.2:c.973C>T (MSH6)	ENSP00000514752.2:p.Gln325Ter
ENST00000699999.1:n.1057C>T (MSH6)
ENST00000700000.1:c.973C>T (MSH6)	ENSP00000514749.1:p.Gln325Ter
ENST00000700002.1:c.979C>T (MSH6)	ENSP00000514750.1:p.Gln327Ter
ENST00000700003.1:c.627+2893C>T (MSH6)	ENSP00000514751.1:n.627+2893C>T
ENST00000700004.1:c.130C>T (MSH6)	ENSP00000514752.1:p.Gln44Ter
ENST00000234420.11:c.973C>T (MSH6) MANE Select	ENSP00000234420.5:p.Gln325Ter
ENST00000540021.6:c.583C>T (MSH6)	ENSP00000446475.1:p.Gln195Ter
ENST00000652107.1:c.676C>T (MSH6)	ENSP00000498629.1:p.Gln226Ter
ENST00000673637.1:c.676C>T (MSH6)	ENSP00000501310.1:p.Gln226Ter
ENST00000234420.9:c.973C>T (MSH6)	ENSP00000234420.4:p.Gln325Ter
ENST00000405808.5:c.169+9239G>A (FBXO11)	ENSP00000385127.1:n.169+9239G>A
ENST00000434234.5:c.*124+9038G>A (FBXO11)	ENSP00000402692.1:n.*124+9038G>A
ENST00000445503.5:c.*320C>T (MSH6)	ENSP00000405294.1:n.*320C>T
ENST00000538136.1:c.67C>T (MSH6)	ENSP00000438580.1:p.Gln23Ter
ENST00000540021.5:c.583C>T (MSH6)	ENSP00000446475.1:p.Gln195Ter
ENST00000614496.4:c.67C>T (MSH6)	ENSP00000477844.1:p.Gln23Ter
ENST00000616033.4:c.970C>T (MSH6)	ENSP00000480261.1:p.Gln324Ter
ENST00000622629.4:c.-2124C>T (MSH6)	ENSP00000482078.1:n.-2124C>T
NM_000179.2:c.973C>T , LRG_219t1:c.973C>T (MSH6)	NP_000170.1:p.Gln325Ter
NM_001281492.1:c.583C>T (MSH6)	NP_001268421.1:p.Gln195Ter
NM_001281493.1:c.67C>T (MSH6)	NP_001268422.1:p.Gln23Ter
NM_001281494.1:c.67C>T (MSH6)	NP_001268423.1:p.Gln23Ter
XM_005264271.1:c.676C>T (MSH6)	XP_005264328.1:p.Gln226Ter
XM_011532798.1:c.790C>T (MSH6)	XP_011531100.1:p.Gln264Ter
XM_011532799.1:c.676C>T (MSH6)	XP_011531101.1:p.Gln226Ter
XM_011532800.1:c.676C>T (MSH6)	XP_011531102.1:p.Gln226Ter
XM_024452819.1:c.973C>T (MSH6)	XP_024308587.1:p.Gln325Ter
XM_024452820.1:c.790C>T (MSH6)	XP_024308588.1:p.Gln264Ter
XM_024452821.1:c.676C>T (MSH6)	XP_024308589.1:p.Gln226Ter
XM_024452822.1:c.67C>T (MSH6)	XP_024308590.1:p.Gln23Ter
NM_000179.3:c.973C>T (MSH6) MANE Select	NP_000170.1:p.Gln325Ter
NM_001281492.2:c.583C>T (MSH6)	NP_001268421.1:p.Gln195Ter
NM_001281493.2:c.67C>T (MSH6)	NP_001268422.1:p.Gln23Ter
NM_001281494.2:c.67C>T (MSH6)	NP_001268423.1:p.Gln23Ter