Canonical Allele Identifier: CA346757838

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1728583
• ClinVar RCV Id: RCV002322786
• dbSNP Id: rs1558386797
• MyVariant Identifiers: chr2:g.48030571G>T (hg19) ; chr2:g.47803432G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803432G>T , CM000664.2:g.47803432G>T	GRCh38
NC_000002.11:g.48030571G>T , CM000664.1:g.48030571G>T	GRCh37
NC_000002.10:g.47884075G>T	NCBI36
NG_007111.1:g.25286G>T , LRG_219:g.25286G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2888G>T (MSH6)	ENSP00000406248.2:p.Cys963Phe
ENST00000420813.6:c.2888G>T (MSH6)	ENSP00000390382.2:p.Cys963Phe
ENST00000455383.6:c.2888G>T (MSH6)	ENSP00000397484.2:p.Cys963Phe
ENST00000700004.2:c.3173-2186G>T (MSH6)	ENSP00000514752.2:n.3173-2186G>T
ENST00000699999.1:n.3269G>T (MSH6)
ENST00000700000.1:c.1619G>T (MSH6)	ENSP00000514749.1:p.Cys540Phe
ENST00000700002.1:c.3191G>T (MSH6)	ENSP00000514750.1:p.Cys1064Phe
ENST00000700003.1:c.640G>T (MSH6)	ENSP00000514751.1:p.Ala214Ser
ENST00000700004.1:c.2330-2186G>T (MSH6)	ENSP00000514752.1:n.2330-2186G>T
ENST00000700005.1:n.2036G>T (MSH6)
ENST00000700006.1:n.2033G>T (MSH6)
ENST00000700007.1:n.1190G>T (MSH6)
ENST00000700008.1:n.764G>T (MSH6)
ENST00000700009.1:n.763G>T (MSH6)
ENST00000700010.1:n.594G>T (MSH6)
ENST00000700011.1:n.665G>T (MSH6)
ENST00000234420.11:c.3185G>T (MSH6) MANE Select	ENSP00000234420.5:p.Cys1062Phe
ENST00000540021.6:c.2795G>T (MSH6)	ENSP00000446475.1:p.Cys932Phe
ENST00000652107.1:c.2888G>T (MSH6)	ENSP00000498629.1:p.Cys963Phe
ENST00000673637.1:c.2888G>T (MSH6)	ENSP00000501310.1:p.Cys963Phe
ENST00000234420.9:c.3185G>T (MSH6)	ENSP00000234420.4:p.Cys1062Phe
ENST00000405808.5:c.169+4763C>A (FBXO11)	ENSP00000385127.1:n.169+4763C>A
ENST00000434234.5:c.*124+4562C>A (FBXO11)	ENSP00000402692.1:n.*124+4562C>A
ENST00000445503.5:c.*2532G>T (MSH6)	ENSP00000405294.1:n.*2532G>T
ENST00000538136.1:c.2279G>T (MSH6)	ENSP00000438580.1:p.Cys760Phe
ENST00000540021.5:c.2795G>T (MSH6)	ENSP00000446475.1:p.Cys932Phe
ENST00000614496.4:c.2279G>T (MSH6)	ENSP00000477844.1:p.Cys760Phe
ENST00000622629.4:c.89G>T (MSH6)	ENSP00000482078.1:p.Cys30Phe
NM_000179.2:c.3185G>T , LRG_219t1:c.3185G>T (MSH6)	NP_000170.1:p.Cys1062Phe
NM_001281492.1:c.2795G>T (MSH6)	NP_001268421.1:p.Cys932Phe
NM_001281493.1:c.2279G>T (MSH6)	NP_001268422.1:p.Cys760Phe
NM_001281494.1:c.2279G>T (MSH6)	NP_001268423.1:p.Cys760Phe
XM_005264271.1:c.2888G>T (MSH6)	XP_005264328.1:p.Cys963Phe
XM_011532798.1:c.3002G>T (MSH6)	XP_011531100.1:p.Cys1001Phe
XM_011532799.1:c.2888G>T (MSH6)	XP_011531101.1:p.Cys963Phe
XM_011532800.1:c.2888G>T (MSH6)	XP_011531102.1:p.Cys963Phe
XM_024452819.1:c.3185G>T (MSH6)	XP_024308587.1:p.Cys1062Phe
XM_024452820.1:c.3002G>T (MSH6)	XP_024308588.1:p.Cys1001Phe
XM_024452821.1:c.2888G>T (MSH6)	XP_024308589.1:p.Cys963Phe
XM_024452822.1:c.2279G>T (MSH6)	XP_024308590.1:p.Cys760Phe
NM_000179.3:c.3185G>T (MSH6) MANE Select	NP_000170.1:p.Cys1062Phe
NM_001281492.2:c.2795G>T (MSH6)	NP_001268421.1:p.Cys932Phe
NM_001281493.2:c.2279G>T (MSH6)	NP_001268422.1:p.Cys760Phe
NM_001281494.2:c.2279G>T (MSH6)	NP_001268423.1:p.Cys760Phe