Canonical Allele Identifier: CA346760496

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 955698
• ClinVar RCV Id: RCV001228382 ; RCV002259096
• dbSNP Id: rs1669959178
• gnomAD v4: 2-47805635-G-A
• MyVariant Identifiers: chr2:g.48032774G>A (hg19) ; chr2:g.47805635G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805635G>A , CM000664.2:g.47805635G>A	GRCh38
NC_000002.11:g.48032774G>A , CM000664.1:g.48032774G>A	GRCh37
NC_000002.10:g.47886278G>A	NCBI36
NG_007111.1:g.27489G>A , LRG_219:g.27489G>A
NG_008397.1:g.105041C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3277G>A (MSH6)	ENSP00000406248.2:p.Val1093Ile
ENST00000420813.6:c.3277G>A (MSH6)	ENSP00000390382.2:p.Val1093Ile
ENST00000455383.6:c.3277G>A (MSH6)	ENSP00000397484.2:p.Val1093Ile
ENST00000700004.2:c.3190G>A (MSH6)	ENSP00000514752.2:p.Val1064Ile
ENST00000699999.1:n.4248G>A (MSH6)
ENST00000700000.1:c.2008G>A (MSH6)	ENSP00000514749.1:p.Val670Ile
ENST00000700002.1:c.3580G>A (MSH6)	ENSP00000514750.1:p.Val1194Ile
ENST00000700003.1:c.1029G>A (MSH6)	ENSP00000514751.1:n.1029G>A
ENST00000700004.1:c.2347G>A (MSH6)	ENSP00000514752.1:p.Val783Ile
ENST00000700005.1:n.2425G>A (MSH6)
ENST00000700006.1:n.4236G>A (MSH6)
ENST00000700007.1:n.2169G>A (MSH6)
ENST00000700008.1:n.1743G>A (MSH6)
ENST00000700009.1:n.1742G>A (MSH6)
ENST00000700010.1:n.983G>A (MSH6)
ENST00000700011.1:n.2868G>A (MSH6)
ENST00000234420.11:c.3574G>A (MSH6) MANE Select	ENSP00000234420.5:p.Val1192Ile
ENST00000540021.6:c.3184G>A (MSH6)	ENSP00000446475.1:p.Val1062Ile
ENST00000652107.1:c.3277G>A (MSH6)	ENSP00000498629.1:p.Val1093Ile
ENST00000673637.1:c.3277G>A (MSH6)	ENSP00000501310.1:p.Val1093Ile
ENST00000234420.9:c.3574G>A (MSH6)	ENSP00000234420.4:p.Val1192Ile
ENST00000405808.5:c.169+2560C>T (FBXO11)	ENSP00000385127.1:n.169+2560C>T
ENST00000434234.5:c.*124+2359C>T (FBXO11)	ENSP00000402692.1:n.*124+2359C>T
ENST00000445503.5:c.*2921G>A (MSH6)	ENSP00000405294.1:n.*2921G>A
ENST00000538136.1:c.2668G>A (MSH6)	ENSP00000438580.1:p.Val890Ile
ENST00000540021.5:c.3184G>A (MSH6)	ENSP00000446475.1:p.Val1062Ile
ENST00000614496.4:c.2668G>A (MSH6)	ENSP00000477844.1:p.Val890Ile
ENST00000622629.4:c.478G>A (MSH6)	ENSP00000482078.1:p.Val160Ile
NM_000179.2:c.3574G>A , LRG_219t1:c.3574G>A (MSH6)	NP_000170.1:p.Val1192Ile
NM_001281492.1:c.3184G>A (MSH6)	NP_001268421.1:p.Val1062Ile
NM_001281493.1:c.2668G>A (MSH6)	NP_001268422.1:p.Val890Ile
NM_001281494.1:c.2668G>A (MSH6)	NP_001268423.1:p.Val890Ile
XM_005264271.1:c.3277G>A (MSH6)	XP_005264328.1:p.Val1093Ile
XM_011532798.1:c.3391G>A (MSH6)	XP_011531100.1:p.Val1131Ile
XM_011532799.1:c.3277G>A (MSH6)	XP_011531101.1:p.Val1093Ile
XM_011532800.1:c.3277G>A (MSH6)	XP_011531102.1:p.Val1093Ile
XM_024452819.1:c.3574G>A (MSH6)	XP_024308587.1:p.Val1192Ile
XM_024452820.1:c.3391G>A (MSH6)	XP_024308588.1:p.Val1131Ile
XM_024452821.1:c.3277G>A (MSH6)	XP_024308589.1:p.Val1093Ile
XM_024452822.1:c.2668G>A (MSH6)	XP_024308590.1:p.Val890Ile
NM_000179.3:c.3574G>A (MSH6) MANE Select	NP_000170.1:p.Val1192Ile
NM_001281492.2:c.3184G>A (MSH6)	NP_001268421.1:p.Val1062Ile
NM_001281493.2:c.2668G>A (MSH6)	NP_001268422.1:p.Val890Ile
NM_001281494.2:c.2668G>A (MSH6)	NP_001268423.1:p.Val890Ile