Canonical Allele Identifier: CA346741935

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48026227A>C (hg19) ; chr2:g.47799088A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799088A>C , CM000664.2:g.47799088A>C	GRCh38
NC_000002.11:g.48026227A>C , CM000664.1:g.48026227A>C	GRCh37
NC_000002.10:g.47879731A>C	NCBI36
NG_007111.1:g.20942A>C , LRG_219:g.20942A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.808A>C (MSH6)	ENSP00000406248.2:p.Thr270Pro
ENST00000420813.6:c.808A>C (MSH6)	ENSP00000390382.2:p.Thr270Pro
ENST00000455383.6:c.808A>C (MSH6)	ENSP00000397484.2:p.Thr270Pro
ENST00000700004.2:c.1105A>C (MSH6)	ENSP00000514752.2:p.Thr369Pro
ENST00000699999.1:n.1189A>C (MSH6)
ENST00000700000.1:c.1105A>C (MSH6)	ENSP00000514749.1:p.Thr369Pro
ENST00000700002.1:c.1111A>C (MSH6)	ENSP00000514750.1:p.Thr371Pro
ENST00000700003.1:c.627+3025A>C (MSH6)	ENSP00000514751.1:n.627+3025A>C
ENST00000700004.1:c.262A>C (MSH6)	ENSP00000514752.1:p.Thr88Pro
ENST00000234420.11:c.1105A>C (MSH6) MANE Select	ENSP00000234420.5:p.Thr369Pro
ENST00000540021.6:c.715A>C (MSH6)	ENSP00000446475.1:p.Thr239Pro
ENST00000652107.1:c.808A>C (MSH6)	ENSP00000498629.1:p.Thr270Pro
ENST00000673637.1:c.808A>C (MSH6)	ENSP00000501310.1:p.Thr270Pro
ENST00000234420.9:c.1105A>C (MSH6)	ENSP00000234420.4:p.Thr369Pro
ENST00000405808.5:c.169+9107T>G (FBXO11)	ENSP00000385127.1:n.169+9107T>G
ENST00000434234.5:c.*124+8906T>G (FBXO11)	ENSP00000402692.1:n.*124+8906T>G
ENST00000445503.5:c.*452A>C (MSH6)	ENSP00000405294.1:n.*452A>C
ENST00000538136.1:c.199A>C (MSH6)	ENSP00000438580.1:p.Thr67Pro
ENST00000540021.5:c.715A>C (MSH6)	ENSP00000446475.1:p.Thr239Pro
ENST00000614496.4:c.199A>C (MSH6)	ENSP00000477844.1:p.Thr67Pro
ENST00000616033.4:c.1102A>C (MSH6)	ENSP00000480261.1:p.Thr368Pro
ENST00000622629.4:c.-1992A>C (MSH6)	ENSP00000482078.1:n.-1992A>C
NM_000179.2:c.1105A>C , LRG_219t1:c.1105A>C (MSH6)	NP_000170.1:p.Thr369Pro
NM_001281492.1:c.715A>C (MSH6)	NP_001268421.1:p.Thr239Pro
NM_001281493.1:c.199A>C (MSH6)	NP_001268422.1:p.Thr67Pro
NM_001281494.1:c.199A>C (MSH6)	NP_001268423.1:p.Thr67Pro
XM_005264271.1:c.808A>C (MSH6)	XP_005264328.1:p.Thr270Pro
XM_011532798.1:c.922A>C (MSH6)	XP_011531100.1:p.Thr308Pro
XM_011532799.1:c.808A>C (MSH6)	XP_011531101.1:p.Thr270Pro
XM_011532800.1:c.808A>C (MSH6)	XP_011531102.1:p.Thr270Pro
XM_024452819.1:c.1105A>C (MSH6)	XP_024308587.1:p.Thr369Pro
XM_024452820.1:c.922A>C (MSH6)	XP_024308588.1:p.Thr308Pro
XM_024452821.1:c.808A>C (MSH6)	XP_024308589.1:p.Thr270Pro
XM_024452822.1:c.199A>C (MSH6)	XP_024308590.1:p.Thr67Pro
NM_000179.3:c.1105A>C (MSH6) MANE Select	NP_000170.1:p.Thr369Pro
NM_001281492.2:c.715A>C (MSH6)	NP_001268421.1:p.Thr239Pro
NM_001281493.2:c.199A>C (MSH6)	NP_001268422.1:p.Thr67Pro
NM_001281494.2:c.199A>C (MSH6)	NP_001268423.1:p.Thr67Pro