Canonical Allele Identifier: CA346761121

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs63751058
• MyVariant Identifiers: chr2:g.48033464T>C (hg19) ; chr2:g.47806325T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47806325T>C , CM000664.2:g.47806325T>C	GRCh38
NC_000002.11:g.48033464T>C , CM000664.1:g.48033464T>C	GRCh37
NC_000002.10:g.47886968T>C	NCBI36
NG_007111.1:g.28179T>C , LRG_219:g.28179T>C
NG_008397.1:g.104351A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3471T>C (MSH6)	ENSP00000406248.2:p.Tyr1157=
ENST00000420813.6:c.3471T>C (MSH6)	ENSP00000390382.2:p.Tyr1157=
ENST00000455383.6:c.3471T>C (MSH6)	ENSP00000397484.2:p.Tyr1157=
ENST00000700004.2:c.3384T>C (MSH6)	ENSP00000514752.2:p.Tyr1128=
ENST00000699999.1:n.4442T>C (MSH6)
ENST00000700000.1:c.2202T>C (MSH6)	ENSP00000514749.1:p.Tyr734=
ENST00000700002.1:c.3774T>C (MSH6)	ENSP00000514750.1:p.Tyr1258=
ENST00000700003.1:c.1223T>C (MSH6)	ENSP00000514751.1:n.1223T>C
ENST00000700004.1:c.2541T>C (MSH6)	ENSP00000514752.1:p.Tyr847=
ENST00000700005.1:n.2619T>C (MSH6)
ENST00000700006.1:n.4926T>C (MSH6)
ENST00000700007.1:n.2363T>C (MSH6)
ENST00000700008.1:n.1937T>C (MSH6)
ENST00000700009.1:n.2432T>C (MSH6)
ENST00000700010.1:n.1177T>C (MSH6)
ENST00000700011.1:n.3062T>C (MSH6)
ENST00000682451.1:n.4423A>G (FBXO11)
ENST00000684712.1:n.4685A>G (FBXO11)
ENST00000234420.11:c.3768T>C (MSH6) MANE Select	ENSP00000234420.5:p.Tyr1256=
ENST00000540021.6:c.3378T>C (MSH6)	ENSP00000446475.1:p.Tyr1126=
ENST00000652107.1:c.3471T>C (MSH6)	ENSP00000498629.1:p.Tyr1157=
ENST00000673637.1:c.3471T>C (MSH6)	ENSP00000501310.1:p.Tyr1157=
ENST00000234420.9:c.3768T>C (MSH6)	ENSP00000234420.4:p.Tyr1256=
ENST00000405808.5:c.169+1870A>G (FBXO11)	ENSP00000385127.1:n.169+1870A>G
ENST00000434234.5:c.*124+1669A>G (FBXO11)	ENSP00000402692.1:n.*124+1669A>G
ENST00000445503.5:c.*3115T>C (MSH6)	ENSP00000405294.1:n.*3115T>C
ENST00000538136.1:c.2862T>C (MSH6)	ENSP00000438580.1:p.Tyr954=
ENST00000540021.5:c.3378T>C (MSH6)	ENSP00000446475.1:p.Tyr1126=
ENST00000614496.4:c.2862T>C (MSH6)	ENSP00000477844.1:p.Tyr954=
ENST00000622629.4:c.670T>C (MSH6)	ENSP00000482078.1:p.Phe224Leu
NM_000179.2:c.3768T>C , LRG_219t1:c.3768T>C (MSH6)	NP_000170.1:p.Tyr1256=
NM_001281492.1:c.3378T>C (MSH6)	NP_001268421.1:p.Tyr1126=
NM_001281493.1:c.2862T>C (MSH6)	NP_001268422.1:p.Tyr954=
NM_001281494.1:c.2862T>C (MSH6)	NP_001268423.1:p.Tyr954=
XM_005264271.1:c.3471T>C (MSH6)	XP_005264328.1:p.Tyr1157=
XM_011532798.1:c.3585T>C (MSH6)	XP_011531100.1:p.Tyr1195=
XM_011532799.1:c.3471T>C (MSH6)	XP_011531101.1:p.Tyr1157=
XM_011532800.1:c.3471T>C (MSH6)	XP_011531102.1:p.Tyr1157=
XM_024452819.1:c.3768T>C (MSH6)	XP_024308587.1:p.Tyr1256=
XM_024452820.1:c.3585T>C (MSH6)	XP_024308588.1:p.Tyr1195=
XM_024452821.1:c.3471T>C (MSH6)	XP_024308589.1:p.Tyr1157=
XM_024452822.1:c.2862T>C (MSH6)	XP_024308590.1:p.Tyr954=
NM_000179.3:c.3768T>C (MSH6) MANE Select	NP_000170.1:p.Tyr1256=
NM_001281492.2:c.3378T>C (MSH6)	NP_001268421.1:p.Tyr1126=
NM_001281493.2:c.2862T>C (MSH6)	NP_001268422.1:p.Tyr954=
NM_001281494.2:c.2862T>C (MSH6)	NP_001268423.1:p.Tyr954=