Canonical Allele Identifier: CA425997270

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48032782A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805643A>G , CM000664.2:g.47805643A>G	GRCh38
NC_000002.11:g.48032782A>G , CM000664.1:g.48032782A>G	GRCh37
NC_000002.10:g.47886286A>G	NCBI36
NG_007111.1:g.27497A>G , LRG_219:g.27497A>G
NG_008397.1:g.105033T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3285A>G (MSH6)	ENSP00000406248.2:p.Leu1095=
ENST00000420813.6:c.3285A>G (MSH6)	ENSP00000390382.2:p.Leu1095=
ENST00000455383.6:c.3285A>G (MSH6)	ENSP00000397484.2:p.Leu1095=
ENST00000700004.2:c.3198A>G (MSH6)	ENSP00000514752.2:p.Leu1066=
ENST00000699999.1:n.4256A>G (MSH6)
ENST00000700000.1:c.2016A>G (MSH6)	ENSP00000514749.1:p.Leu672=
ENST00000700002.1:c.3588A>G (MSH6)	ENSP00000514750.1:p.Leu1196=
ENST00000700003.1:c.1037A>G (MSH6)	ENSP00000514751.1:n.1037A>G
ENST00000700004.1:c.2355A>G (MSH6)	ENSP00000514752.1:p.Leu785=
ENST00000700005.1:n.2433A>G (MSH6)
ENST00000700006.1:n.4244A>G (MSH6)
ENST00000700007.1:n.2177A>G (MSH6)
ENST00000700008.1:n.1751A>G (MSH6)
ENST00000700009.1:n.1750A>G (MSH6)
ENST00000700010.1:n.991A>G (MSH6)
ENST00000700011.1:n.2876A>G (MSH6)
ENST00000234420.11:c.3582A>G (MSH6) MANE Select	ENSP00000234420.5:p.Leu1194=
ENST00000540021.6:c.3192A>G (MSH6)	ENSP00000446475.1:p.Leu1064=
ENST00000652107.1:c.3285A>G (MSH6)	ENSP00000498629.1:p.Leu1095=
ENST00000673637.1:c.3285A>G (MSH6)	ENSP00000501310.1:p.Leu1095=
ENST00000234420.9:c.3582A>G (MSH6)	ENSP00000234420.4:p.Leu1194=
ENST00000405808.5:c.169+2552T>C (FBXO11)	ENSP00000385127.1:n.169+2552T>C
ENST00000434234.5:c.*124+2351T>C (FBXO11)	ENSP00000402692.1:n.*124+2351T>C
ENST00000445503.5:c.*2929A>G (MSH6)	ENSP00000405294.1:n.*2929A>G
ENST00000538136.1:c.2676A>G (MSH6)	ENSP00000438580.1:p.Leu892=
ENST00000540021.5:c.3192A>G (MSH6)	ENSP00000446475.1:p.Leu1064=
ENST00000614496.4:c.2676A>G (MSH6)	ENSP00000477844.1:p.Leu892=
ENST00000622629.4:c.486A>G (MSH6)	ENSP00000482078.1:p.Leu162=
NM_000179.2:c.3582A>G , LRG_219t1:c.3582A>G (MSH6)	NP_000170.1:p.Leu1194=
NM_001281492.1:c.3192A>G (MSH6)	NP_001268421.1:p.Leu1064=
NM_001281493.1:c.2676A>G (MSH6)	NP_001268422.1:p.Leu892=
NM_001281494.1:c.2676A>G (MSH6)	NP_001268423.1:p.Leu892=
XM_005264271.1:c.3285A>G (MSH6)	XP_005264328.1:p.Leu1095=
XM_011532798.1:c.3399A>G (MSH6)	XP_011531100.1:p.Leu1133=
XM_011532799.1:c.3285A>G (MSH6)	XP_011531101.1:p.Leu1095=
XM_011532800.1:c.3285A>G (MSH6)	XP_011531102.1:p.Leu1095=
XM_024452819.1:c.3582A>G (MSH6)	XP_024308587.1:p.Leu1194=
XM_024452820.1:c.3399A>G (MSH6)	XP_024308588.1:p.Leu1133=
XM_024452821.1:c.3285A>G (MSH6)	XP_024308589.1:p.Leu1095=
XM_024452822.1:c.2676A>G (MSH6)	XP_024308590.1:p.Leu892=
NM_000179.3:c.3582A>G (MSH6) MANE Select	NP_000170.1:p.Leu1194=
NM_001281492.2:c.3192A>G (MSH6)	NP_001268421.1:p.Leu1064=
NM_001281493.2:c.2676A>G (MSH6)	NP_001268422.1:p.Leu892=
NM_001281494.2:c.2676A>G (MSH6)	NP_001268423.1:p.Leu892=