Canonical Allele Identifier: CA426122156

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 2773670
• ClinVar RCV Id: RCV003585643
• MyVariant Identifiers: chr2:g.48033707T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806568T>A , CM000664.2:g.47806568T>A	GRCh38
NC_000002.11:g.48033707T>A , CM000664.1:g.48033707T>A	GRCh37
NC_000002.10:g.47887211T>A	NCBI36
NG_007111.1:g.28422T>A , LRG_219:g.28422T>A
NG_008397.1:g.104108A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3621T>A (MSH6)	ENSP00000406248.2:p.Ala1207=
ENST00000420813.6:c.3621T>A (MSH6)	ENSP00000390382.2:p.Ala1207=
ENST00000455383.6:c.3621T>A (MSH6)	ENSP00000397484.2:p.Ala1207=
ENST00000700004.2:c.3534T>A (MSH6)	ENSP00000514752.2:p.Ala1178=
ENST00000699999.1:n.4592T>A (MSH6)
ENST00000700000.1:c.2352T>A (MSH6)	ENSP00000514749.1:p.Ala784=
ENST00000700002.1:c.3924T>A (MSH6)	ENSP00000514750.1:p.Ala1308=
ENST00000700003.1:c.1373T>A (MSH6)	ENSP00000514751.1:n.1373T>A
ENST00000700004.1:c.2691T>A (MSH6)	ENSP00000514752.1:p.Ala897=
ENST00000700005.1:n.2769T>A (MSH6)
ENST00000700006.1:n.5076T>A (MSH6)
ENST00000700007.1:n.2513T>A (MSH6)
ENST00000700008.1:n.2180T>A (MSH6)
ENST00000700009.1:n.2582T>A (MSH6)
ENST00000700010.1:n.1327T>A (MSH6)
ENST00000700011.1:n.3212T>A (MSH6)
ENST00000682451.1:n.4180A>T (FBXO11)
ENST00000684712.1:n.4442A>T (FBXO11)
ENST00000234420.11:c.3918T>A (MSH6) MANE Select	ENSP00000234420.5:p.Ala1306=
ENST00000540021.6:c.3528T>A (MSH6)	ENSP00000446475.1:p.Ala1176=
ENST00000652107.1:c.3621T>A (MSH6)	ENSP00000498629.1:p.Ala1207=
ENST00000673637.1:c.3621T>A (MSH6)	ENSP00000501310.1:p.Ala1207=
ENST00000234420.9:c.3918T>A (MSH6)	ENSP00000234420.4:p.Ala1306=
ENST00000405808.5:c.169+1627A>T (FBXO11)	ENSP00000385127.1:n.169+1627A>T
ENST00000434234.5:c.*124+1426A>T (FBXO11)	ENSP00000402692.1:n.*124+1426A>T
ENST00000445503.5:c.*3265T>A (MSH6)	ENSP00000405294.1:n.*3265T>A
ENST00000538136.1:c.3012T>A (MSH6)	ENSP00000438580.1:p.Ala1004=
ENST00000540021.5:c.3528T>A (MSH6)	ENSP00000446475.1:p.Ala1176=
ENST00000614496.4:c.3012T>A (MSH6)	ENSP00000477844.1:p.Ala1004=
ENST00000622629.4:c.819T>A (MSH6)	ENSP00000482078.1:p.Ala273=
NM_000179.2:c.3918T>A , LRG_219t1:c.3918T>A (MSH6)	NP_000170.1:p.Ala1306=
NM_001281492.1:c.3528T>A (MSH6)	NP_001268421.1:p.Ala1176=
NM_001281493.1:c.3012T>A (MSH6)	NP_001268422.1:p.Ala1004=
NM_001281494.1:c.3012T>A (MSH6)	NP_001268423.1:p.Ala1004=
XM_005264271.1:c.3621T>A (MSH6)	XP_005264328.1:p.Ala1207=
XM_011532798.1:c.3735T>A (MSH6)	XP_011531100.1:p.Ala1245=
XM_011532799.1:c.3621T>A (MSH6)	XP_011531101.1:p.Ala1207=
XM_011532800.1:c.3621T>A (MSH6)	XP_011531102.1:p.Ala1207=
XM_024452819.1:c.4011T>A (MSH6)	XP_024308587.1:p.Ala1337=
XM_024452820.1:c.3828T>A (MSH6)	XP_024308588.1:p.Ala1276=
XM_024452821.1:c.3714T>A (MSH6)	XP_024308589.1:p.Ala1238=
XM_024452822.1:c.3105T>A (MSH6)	XP_024308590.1:p.Ala1035=
NM_000179.3:c.3918T>A (MSH6) MANE Select	NP_000170.1:p.Ala1306=
NM_001281492.2:c.3528T>A (MSH6)	NP_001268421.1:p.Ala1176=
NM_001281493.2:c.3012T>A (MSH6)	NP_001268422.1:p.Ala1004=
NM_001281494.2:c.3012T>A (MSH6)	NP_001268423.1:p.Ala1004=