Canonical Allele Identifier: CA426120733

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 763438
• ClinVar RCV Id: RCV001472439
• dbSNP Id: rs1572721207
• MyVariant Identifiers: chr2:g.48026121C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798982C>G , CM000664.2:g.47798982C>G	GRCh38
NC_000002.11:g.48026121C>G , CM000664.1:g.48026121C>G	GRCh37
NC_000002.10:g.47879625C>G	NCBI36
NG_007111.1:g.20836C>G , LRG_219:g.20836C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.702C>G (MSH6)	ENSP00000406248.2:p.Thr234=
ENST00000420813.6:c.702C>G (MSH6)	ENSP00000390382.2:p.Thr234=
ENST00000455383.6:c.702C>G (MSH6)	ENSP00000397484.2:p.Thr234=
ENST00000700004.2:c.999C>G (MSH6)	ENSP00000514752.2:p.Thr333=
ENST00000699999.1:n.1083C>G (MSH6)
ENST00000700000.1:c.999C>G (MSH6)	ENSP00000514749.1:p.Thr333=
ENST00000700002.1:c.1005C>G (MSH6)	ENSP00000514750.1:p.Thr335=
ENST00000700003.1:c.627+2919C>G (MSH6)	ENSP00000514751.1:n.627+2919C>G
ENST00000700004.1:c.156C>G (MSH6)	ENSP00000514752.1:p.Thr52=
ENST00000234420.11:c.999C>G (MSH6) MANE Select	ENSP00000234420.5:p.Thr333=
ENST00000540021.6:c.609C>G (MSH6)	ENSP00000446475.1:p.Thr203=
ENST00000652107.1:c.702C>G (MSH6)	ENSP00000498629.1:p.Thr234=
ENST00000673637.1:c.702C>G (MSH6)	ENSP00000501310.1:p.Thr234=
ENST00000234420.9:c.999C>G (MSH6)	ENSP00000234420.4:p.Thr333=
ENST00000405808.5:c.169+9213G>C (FBXO11)	ENSP00000385127.1:n.169+9213G>C
ENST00000434234.5:c.*124+9012G>C (FBXO11)	ENSP00000402692.1:n.*124+9012G>C
ENST00000445503.5:c.*346C>G (MSH6)	ENSP00000405294.1:n.*346C>G
ENST00000538136.1:c.93C>G (MSH6)	ENSP00000438580.1:p.Thr31=
ENST00000540021.5:c.609C>G (MSH6)	ENSP00000446475.1:p.Thr203=
ENST00000614496.4:c.93C>G (MSH6)	ENSP00000477844.1:p.Thr31=
ENST00000616033.4:c.996C>G (MSH6)	ENSP00000480261.1:p.Thr332=
ENST00000622629.4:c.-2098C>G (MSH6)	ENSP00000482078.1:n.-2098C>G
NM_000179.2:c.999C>G , LRG_219t1:c.999C>G (MSH6)	NP_000170.1:p.Thr333=
NM_001281492.1:c.609C>G (MSH6)	NP_001268421.1:p.Thr203=
NM_001281493.1:c.93C>G (MSH6)	NP_001268422.1:p.Thr31=
NM_001281494.1:c.93C>G (MSH6)	NP_001268423.1:p.Thr31=
XM_005264271.1:c.702C>G (MSH6)	XP_005264328.1:p.Thr234=
XM_011532798.1:c.816C>G (MSH6)	XP_011531100.1:p.Thr272=
XM_011532799.1:c.702C>G (MSH6)	XP_011531101.1:p.Thr234=
XM_011532800.1:c.702C>G (MSH6)	XP_011531102.1:p.Thr234=
XM_024452819.1:c.999C>G (MSH6)	XP_024308587.1:p.Thr333=
XM_024452820.1:c.816C>G (MSH6)	XP_024308588.1:p.Thr272=
XM_024452821.1:c.702C>G (MSH6)	XP_024308589.1:p.Thr234=
XM_024452822.1:c.93C>G (MSH6)	XP_024308590.1:p.Thr31=
NM_000179.3:c.999C>G (MSH6) MANE Select	NP_000170.1:p.Thr333=
NM_001281492.2:c.609C>G (MSH6)	NP_001268421.1:p.Thr203=
NM_001281493.2:c.93C>G (MSH6)	NP_001268422.1:p.Thr31=
NM_001281494.2:c.93C>G (MSH6)	NP_001268423.1:p.Thr31=