Canonical Allele Identifier: CA016437

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 89566
• ClinVar RCV Id: RCV000075035 ; RCV001354709 ; RCV003450992
• dbSNP Id: rs267608048
• MyVariant Identifiers: chr2:g.48025877C>G (hg19) ; chr2:g.47798738C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798738C>G , CM000664.2:g.47798738C>G	GRCh38
NC_000002.11:g.48025877C>G , CM000664.1:g.48025877C>G	GRCh37
NC_000002.10:g.47879381C>G	NCBI36
NG_007111.1:g.20592C>G , LRG_219:g.20592C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.458C>G (MSH6)	ENSP00000406248.2:p.Ser153Ter
ENST00000420813.6:c.458C>G (MSH6)	ENSP00000390382.2:p.Ser153Ter
ENST00000455383.6:c.458C>G (MSH6)	ENSP00000397484.2:p.Ser153Ter
ENST00000700004.2:c.755C>G (MSH6)	ENSP00000514752.2:p.Ser252Ter
ENST00000699999.1:n.839C>G (MSH6)
ENST00000700000.1:c.755C>G (MSH6)	ENSP00000514749.1:p.Ser252Ter
ENST00000700002.1:c.761C>G (MSH6)	ENSP00000514750.1:p.Ser254Ter
ENST00000700003.1:c.627+2675C>G (MSH6)	ENSP00000514751.1:n.627+2675C>G
ENST00000234420.11:c.755C>G (MSH6) MANE Select	ENSP00000234420.5:p.Ser252Ter
ENST00000540021.6:c.365C>G (MSH6)	ENSP00000446475.1:p.Ser122Ter
ENST00000652107.1:c.458C>G (MSH6)	ENSP00000498629.1:p.Ser153Ter
ENST00000673637.1:c.458C>G (MSH6)	ENSP00000501310.1:p.Ser153Ter
ENST00000673922.1:n.477C>G (MSH6)
ENST00000234420.9:c.755C>G (MSH6)	ENSP00000234420.4:p.Ser252Ter
ENST00000405808.5:c.170-9298G>C (FBXO11)	ENSP00000385127.1:n.170-9298G>C
ENST00000434234.5:c.*124+9256G>C (FBXO11)	ENSP00000402692.1:n.*124+9256G>C
ENST00000445503.5:c.*102C>G (MSH6)	ENSP00000405294.1:n.*102C>G
ENST00000456246.1:c.*243C>G (MSH6)	ENSP00000410570.1:n.*243C>G
ENST00000538136.1:c.-152C>G (MSH6)	ENSP00000438580.1:n.-152C>G
ENST00000540021.5:c.365C>G (MSH6)	ENSP00000446475.1:p.Ser122Ter
ENST00000614496.4:c.-152C>G (MSH6)	ENSP00000477844.1:n.-152C>G
ENST00000616033.4:c.752C>G (MSH6)	ENSP00000480261.1:p.Ser251Ter
ENST00000622629.4:c.-2342C>G (MSH6)	ENSP00000482078.1:n.-2342C>G
NM_000179.2:c.755C>G , LRG_219t1:c.755C>G (MSH6)	NP_000170.1:p.Ser252Ter
NM_001281492.1:c.365C>G (MSH6)	NP_001268421.1:p.Ser122Ter
NM_001281493.1:c.-152C>G (MSH6)	NP_001268422.1:n.-152C>G
NM_001281494.1:c.-152C>G (MSH6)	NP_001268423.1:n.-152C>G
XM_005264271.1:c.458C>G (MSH6)	XP_005264328.1:p.Ser153Ter
XM_011532798.1:c.572C>G (MSH6)	XP_011531100.1:p.Ser191Ter
XM_011532799.1:c.458C>G (MSH6)	XP_011531101.1:p.Ser153Ter
XM_011532800.1:c.458C>G (MSH6)	XP_011531102.1:p.Ser153Ter
XM_024452819.1:c.755C>G (MSH6)	XP_024308587.1:p.Ser252Ter
XM_024452820.1:c.572C>G (MSH6)	XP_024308588.1:p.Ser191Ter
XM_024452821.1:c.458C>G (MSH6)	XP_024308589.1:p.Ser153Ter
XM_024452822.1:c.-152C>G (MSH6)	XP_024308590.1:n.-152C>G
NM_000179.3:c.755C>G (MSH6) MANE Select	NP_000170.1:p.Ser252Ter
NM_001281492.2:c.365C>G (MSH6)	NP_001268421.1:p.Ser122Ter
NM_001281493.2:c.-152C>G (MSH6)	NP_001268422.1:n.-152C>G
NM_001281494.2:c.-152C>G (MSH6)	NP_001268423.1:n.-152C>G