Canonical Allele Identifier: CA426120955

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48026001T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798862T>G , CM000664.2:g.47798862T>G	GRCh38
NC_000002.11:g.48026001T>G , CM000664.1:g.48026001T>G	GRCh37
NC_000002.10:g.47879505T>G	NCBI36
NG_007111.1:g.20716T>G , LRG_219:g.20716T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.582T>G (MSH6)	ENSP00000406248.2:p.Pro194=
ENST00000420813.6:c.582T>G (MSH6)	ENSP00000390382.2:p.Pro194=
ENST00000455383.6:c.582T>G (MSH6)	ENSP00000397484.2:p.Pro194=
ENST00000700004.2:c.879T>G (MSH6)	ENSP00000514752.2:p.Pro293=
ENST00000699999.1:n.963T>G (MSH6)
ENST00000700000.1:c.879T>G (MSH6)	ENSP00000514749.1:p.Pro293=
ENST00000700002.1:c.885T>G (MSH6)	ENSP00000514750.1:p.Pro295=
ENST00000700003.1:c.627+2799T>G (MSH6)	ENSP00000514751.1:n.627+2799T>G
ENST00000700004.1:c.36T>G (MSH6)	ENSP00000514752.1:p.Pro12=
ENST00000234420.11:c.879T>G (MSH6) MANE Select	ENSP00000234420.5:p.Pro293=
ENST00000540021.6:c.489T>G (MSH6)	ENSP00000446475.1:p.Pro163=
ENST00000652107.1:c.582T>G (MSH6)	ENSP00000498629.1:p.Pro194=
ENST00000673637.1:c.582T>G (MSH6)	ENSP00000501310.1:p.Pro194=
ENST00000234420.9:c.879T>G (MSH6)	ENSP00000234420.4:p.Pro293=
ENST00000405808.5:c.169+9333A>C (FBXO11)	ENSP00000385127.1:n.169+9333A>C
ENST00000434234.5:c.*124+9132A>C (FBXO11)	ENSP00000402692.1:n.*124+9132A>C
ENST00000445503.5:c.*226T>G (MSH6)	ENSP00000405294.1:n.*226T>G
ENST00000456246.1:c.*367T>G (MSH6)	ENSP00000410570.1:n.*367T>G
ENST00000538136.1:c.-28T>G (MSH6)	ENSP00000438580.1:n.-28T>G
ENST00000540021.5:c.489T>G (MSH6)	ENSP00000446475.1:p.Pro163=
ENST00000614496.4:c.-28T>G (MSH6)	ENSP00000477844.1:n.-28T>G
ENST00000616033.4:c.876T>G (MSH6)	ENSP00000480261.1:p.Pro292=
ENST00000622629.4:c.-2218T>G (MSH6)	ENSP00000482078.1:n.-2218T>G
NM_000179.2:c.879T>G , LRG_219t1:c.879T>G (MSH6)	NP_000170.1:p.Pro293=
NM_001281492.1:c.489T>G (MSH6)	NP_001268421.1:p.Pro163=
NM_001281493.1:c.-28T>G (MSH6)	NP_001268422.1:n.-28T>G
NM_001281494.1:c.-28T>G (MSH6)	NP_001268423.1:n.-28T>G
XM_005264271.1:c.582T>G (MSH6)	XP_005264328.1:p.Pro194=
XM_011532798.1:c.696T>G (MSH6)	XP_011531100.1:p.Pro232=
XM_011532799.1:c.582T>G (MSH6)	XP_011531101.1:p.Pro194=
XM_011532800.1:c.582T>G (MSH6)	XP_011531102.1:p.Pro194=
XM_024452819.1:c.879T>G (MSH6)	XP_024308587.1:p.Pro293=
XM_024452820.1:c.696T>G (MSH6)	XP_024308588.1:p.Pro232=
XM_024452821.1:c.582T>G (MSH6)	XP_024308589.1:p.Pro194=
XM_024452822.1:c.-28T>G (MSH6)	XP_024308590.1:n.-28T>G
NM_000179.3:c.879T>G (MSH6) MANE Select	NP_000170.1:p.Pro293=
NM_001281492.2:c.489T>G (MSH6)	NP_001268421.1:p.Pro163=
NM_001281493.2:c.-28T>G (MSH6)	NP_001268422.1:n.-28T>G
NM_001281494.2:c.-28T>G (MSH6)	NP_001268423.1:n.-28T>G