Canonical Allele Identifier: CA346760137

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48032092C>A (hg19) ; chr2:g.47804953C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804953C>A , CM000664.2:g.47804953C>A	GRCh38
NC_000002.11:g.48032092C>A , CM000664.1:g.48032092C>A	GRCh37
NC_000002.10:g.47885596C>A	NCBI36
NG_007111.1:g.26807C>A , LRG_219:g.26807C>A
NG_008397.1:g.105723G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3185C>A (MSH6)	ENSP00000406248.2:p.Pro1062His
ENST00000420813.6:c.3185C>A (MSH6)	ENSP00000390382.2:p.Pro1062His
ENST00000455383.6:c.3185C>A (MSH6)	ENSP00000397484.2:p.Pro1062His
ENST00000700004.2:c.3173-665C>A (MSH6)	ENSP00000514752.2:n.3173-665C>A
ENST00000699999.1:n.3566C>A (MSH6)
ENST00000700000.1:c.1916C>A (MSH6)	ENSP00000514749.1:p.Pro639His
ENST00000700002.1:c.3488C>A (MSH6)	ENSP00000514750.1:p.Pro1163His
ENST00000700003.1:c.937C>A (MSH6)	ENSP00000514751.1:n.937C>A
ENST00000700004.1:c.2330-665C>A (MSH6)	ENSP00000514752.1:n.2330-665C>A
ENST00000700005.1:n.2333C>A (MSH6)
ENST00000700006.1:n.3554C>A (MSH6)
ENST00000700007.1:n.1487C>A (MSH6)
ENST00000700008.1:n.1061C>A (MSH6)
ENST00000700009.1:n.1060C>A (MSH6)
ENST00000700010.1:n.891C>A (MSH6)
ENST00000700011.1:n.2186C>A (MSH6)
ENST00000234420.11:c.3482C>A (MSH6) MANE Select	ENSP00000234420.5:p.Pro1161His
ENST00000540021.6:c.3092C>A (MSH6)	ENSP00000446475.1:p.Pro1031His
ENST00000652107.1:c.3185C>A (MSH6)	ENSP00000498629.1:p.Pro1062His
ENST00000673637.1:c.3185C>A (MSH6)	ENSP00000501310.1:p.Pro1062His
ENST00000234420.9:c.3482C>A (MSH6)	ENSP00000234420.4:p.Pro1161His
ENST00000405808.5:c.169+3242G>T (FBXO11)	ENSP00000385127.1:n.169+3242G>T
ENST00000434234.5:c.*124+3041G>T (FBXO11)	ENSP00000402692.1:n.*124+3041G>T
ENST00000445503.5:c.*2829C>A (MSH6)	ENSP00000405294.1:n.*2829C>A
ENST00000538136.1:c.2576C>A (MSH6)	ENSP00000438580.1:p.Pro859His
ENST00000540021.5:c.3092C>A (MSH6)	ENSP00000446475.1:p.Pro1031His
ENST00000614496.4:c.2576C>A (MSH6)	ENSP00000477844.1:p.Pro859His
ENST00000622629.4:c.386C>A (MSH6)	ENSP00000482078.1:p.Pro129His
NM_000179.2:c.3482C>A , LRG_219t1:c.3482C>A (MSH6)	NP_000170.1:p.Pro1161His
NM_001281492.1:c.3092C>A (MSH6)	NP_001268421.1:p.Pro1031His
NM_001281493.1:c.2576C>A (MSH6)	NP_001268422.1:p.Pro859His
NM_001281494.1:c.2576C>A (MSH6)	NP_001268423.1:p.Pro859His
XM_005264271.1:c.3185C>A (MSH6)	XP_005264328.1:p.Pro1062His
XM_011532798.1:c.3299C>A (MSH6)	XP_011531100.1:p.Pro1100His
XM_011532799.1:c.3185C>A (MSH6)	XP_011531101.1:p.Pro1062His
XM_011532800.1:c.3185C>A (MSH6)	XP_011531102.1:p.Pro1062His
XM_024452819.1:c.3482C>A (MSH6)	XP_024308587.1:p.Pro1161His
XM_024452820.1:c.3299C>A (MSH6)	XP_024308588.1:p.Pro1100His
XM_024452821.1:c.3185C>A (MSH6)	XP_024308589.1:p.Pro1062His
XM_024452822.1:c.2576C>A (MSH6)	XP_024308590.1:p.Pro859His
NM_000179.3:c.3482C>A (MSH6) MANE Select	NP_000170.1:p.Pro1161His
NM_001281492.2:c.3092C>A (MSH6)	NP_001268421.1:p.Pro1031His
NM_001281493.2:c.2576C>A (MSH6)	NP_001268422.1:p.Pro859His
NM_001281494.2:c.2576C>A (MSH6)	NP_001268423.1:p.Pro859His