Canonical Allele Identifier: CA346761382

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs2104558109
• MyVariant Identifiers: chr2:g.48033672C>G (hg19) ; chr2:g.47806533C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806533C>G , CM000664.2:g.47806533C>G	GRCh38
NC_000002.11:g.48033672C>G , CM000664.1:g.48033672C>G	GRCh37
NC_000002.10:g.47887176C>G	NCBI36
NG_007111.1:g.28387C>G , LRG_219:g.28387C>G
NG_008397.1:g.104143G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3586C>G (MSH6)	ENSP00000406248.2:p.Pro1196Ala
ENST00000420813.6:c.3586C>G (MSH6)	ENSP00000390382.2:p.Pro1196Ala
ENST00000455383.6:c.3586C>G (MSH6)	ENSP00000397484.2:p.Pro1196Ala
ENST00000700004.2:c.3499C>G (MSH6)	ENSP00000514752.2:p.Pro1167Ala
ENST00000699999.1:n.4557C>G (MSH6)
ENST00000700000.1:c.2317C>G (MSH6)	ENSP00000514749.1:p.Pro773Ala
ENST00000700002.1:c.3889C>G (MSH6)	ENSP00000514750.1:p.Pro1297Ala
ENST00000700003.1:c.1338C>G (MSH6)	ENSP00000514751.1:n.1338C>G
ENST00000700004.1:c.2656C>G (MSH6)	ENSP00000514752.1:p.Pro886Ala
ENST00000700005.1:n.2734C>G (MSH6)
ENST00000700006.1:n.5041C>G (MSH6)
ENST00000700007.1:n.2478C>G (MSH6)
ENST00000700008.1:n.2145C>G (MSH6)
ENST00000700009.1:n.2547C>G (MSH6)
ENST00000700010.1:n.1292C>G (MSH6)
ENST00000700011.1:n.3177C>G (MSH6)
ENST00000682451.1:n.4215G>C (FBXO11)
ENST00000684712.1:n.4477G>C (FBXO11)
ENST00000234420.11:c.3883C>G (MSH6) MANE Select	ENSP00000234420.5:p.Pro1295Ala
ENST00000540021.6:c.3493C>G (MSH6)	ENSP00000446475.1:p.Pro1165Ala
ENST00000652107.1:c.3586C>G (MSH6)	ENSP00000498629.1:p.Pro1196Ala
ENST00000673637.1:c.3586C>G (MSH6)	ENSP00000501310.1:p.Pro1196Ala
ENST00000234420.9:c.3883C>G (MSH6)	ENSP00000234420.4:p.Pro1295Ala
ENST00000405808.5:c.169+1662G>C (FBXO11)	ENSP00000385127.1:n.169+1662G>C
ENST00000434234.5:c.*124+1461G>C (FBXO11)	ENSP00000402692.1:n.*124+1461G>C
ENST00000445503.5:c.*3230C>G (MSH6)	ENSP00000405294.1:n.*3230C>G
ENST00000538136.1:c.2977C>G (MSH6)	ENSP00000438580.1:p.Pro993Ala
ENST00000540021.5:c.3493C>G (MSH6)	ENSP00000446475.1:p.Pro1165Ala
ENST00000614496.4:c.2977C>G (MSH6)	ENSP00000477844.1:p.Pro993Ala
ENST00000622629.4:c.784C>G (MSH6)	ENSP00000482078.1:p.Pro262Ala
NM_000179.2:c.3883C>G , LRG_219t1:c.3883C>G (MSH6)	NP_000170.1:p.Pro1295Ala
NM_001281492.1:c.3493C>G (MSH6)	NP_001268421.1:p.Pro1165Ala
NM_001281493.1:c.2977C>G (MSH6)	NP_001268422.1:p.Pro993Ala
NM_001281494.1:c.2977C>G (MSH6)	NP_001268423.1:p.Pro993Ala
XM_005264271.1:c.3586C>G (MSH6)	XP_005264328.1:p.Pro1196Ala
XM_011532798.1:c.3700C>G (MSH6)	XP_011531100.1:p.Pro1234Ala
XM_011532799.1:c.3586C>G (MSH6)	XP_011531101.1:p.Pro1196Ala
XM_011532800.1:c.3586C>G (MSH6)	XP_011531102.1:p.Pro1196Ala
XM_024452819.1:c.3976C>G (MSH6)	XP_024308587.1:p.Pro1326Ala
XM_024452820.1:c.3793C>G (MSH6)	XP_024308588.1:p.Pro1265Ala
XM_024452821.1:c.3679C>G (MSH6)	XP_024308589.1:p.Pro1227Ala
XM_024452822.1:c.3070C>G (MSH6)	XP_024308590.1:p.Pro1024Ala
NM_000179.3:c.3883C>G (MSH6) MANE Select	NP_000170.1:p.Pro1295Ala
NM_001281492.2:c.3493C>G (MSH6)	NP_001268421.1:p.Pro1165Ala
NM_001281493.2:c.2977C>G (MSH6)	NP_001268422.1:p.Pro993Ala
NM_001281494.2:c.2977C>G (MSH6)	NP_001268423.1:p.Pro993Ala