Canonical Allele Identifier: CA346756752

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 428291
• ClinVar RCV Id: RCV000491302 ; RCV001390928 ; RCV003449283
• dbSNP Id: rs587779255
• COSMIC: COSM6475201
• MyVariant Identifiers: chr2:g.48028295G>A (hg19) ; chr2:g.47801156G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47801156G>A , CM000664.2:g.47801156G>A	GRCh38
NC_000002.11:g.48028295G>A , CM000664.1:g.48028295G>A	GRCh37
NC_000002.10:g.47881799G>A	NCBI36
NG_007111.1:g.23010G>A , LRG_219:g.23010G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2875+1G>A (MSH6)	ENSP00000406248.2:n.2875+1G>A
ENST00000420813.6:c.2875+1G>A (MSH6)	ENSP00000390382.2:n.2875+1G>A
ENST00000455383.6:c.2875+1G>A (MSH6)	ENSP00000397484.2:n.2875+1G>A
ENST00000700004.2:c.3172+1G>A (MSH6)	ENSP00000514752.2:n.3172+1G>A
ENST00000699999.1:n.3256+1G>A (MSH6)
ENST00000700000.1:c.1606+1567G>A (MSH6)	ENSP00000514749.1:n.1606+1567G>A
ENST00000700002.1:c.3178+1G>A (MSH6)	ENSP00000514750.1:n.3178+1G>A
ENST00000700003.1:c.628-2264G>A (MSH6)	ENSP00000514751.1:n.628-2264G>A
ENST00000700004.1:c.2329+1G>A (MSH6)	ENSP00000514752.1:n.2329+1G>A
ENST00000234420.11:c.3172+1G>A (MSH6) MANE Select	ENSP00000234420.5:n.3172+1G>A
ENST00000540021.6:c.2782+1G>A (MSH6)	ENSP00000446475.1:n.2782+1G>A
ENST00000652107.1:c.2875+1G>A (MSH6)	ENSP00000498629.1:n.2875+1G>A
ENST00000673637.1:c.2875+1G>A (MSH6)	ENSP00000501310.1:n.2875+1G>A
ENST00000234420.9:c.3172+1G>A (MSH6)	ENSP00000234420.4:n.3172+1G>A
ENST00000405808.5:c.169+7039C>T (FBXO11)	ENSP00000385127.1:n.169+7039C>T
ENST00000434234.5:c.*124+6838C>T (FBXO11)	ENSP00000402692.1:n.*124+6838C>T
ENST00000445503.5:c.*2519+1G>A (MSH6)	ENSP00000405294.1:n.*2519+1G>A
ENST00000538136.1:c.2266+1G>A (MSH6)	ENSP00000438580.1:n.2266+1G>A
ENST00000540021.5:c.2782+1G>A (MSH6)	ENSP00000446475.1:n.2782+1G>A
ENST00000614496.4:c.2266+1G>A (MSH6)	ENSP00000477844.1:n.2266+1G>A
ENST00000616033.4:c.3170G>A (MSH6)	ENSP00000480261.1:p.Gly1057Asp
ENST00000622629.4:c.76+1G>A (MSH6)	ENSP00000482078.1:n.76+1G>A
NM_000179.2:c.3172+1G>A , LRG_219t1:c.3172+1G>A (MSH6)	NP_000170.1:n.3172+1G>A
NM_001281492.1:c.2782+1G>A (MSH6)	NP_001268421.1:n.2782+1G>A
NM_001281493.1:c.2266+1G>A (MSH6)	NP_001268422.1:n.2266+1G>A
NM_001281494.1:c.2266+1G>A (MSH6)	NP_001268423.1:n.2266+1G>A
XM_005264271.1:c.2875+1G>A (MSH6)	XP_005264328.1:n.2875+1G>A
XM_011532798.1:c.2989+1G>A (MSH6)	XP_011531100.1:n.2989+1G>A
XM_011532799.1:c.2875+1G>A (MSH6)	XP_011531101.1:n.2875+1G>A
XM_011532800.1:c.2875+1G>A (MSH6)	XP_011531102.1:n.2875+1G>A
XM_024452819.1:c.3172+1G>A (MSH6)	XP_024308587.1:n.3172+1G>A
XM_024452820.1:c.2989+1G>A (MSH6)	XP_024308588.1:n.2989+1G>A
XM_024452821.1:c.2875+1G>A (MSH6)	XP_024308589.1:n.2875+1G>A
XM_024452822.1:c.2266+1G>A (MSH6)	XP_024308590.1:n.2266+1G>A
NM_000179.3:c.3172+1G>A (MSH6) MANE Select	NP_000170.1:n.3172+1G>A
NM_001281492.2:c.2782+1G>A (MSH6)	NP_001268421.1:n.2782+1G>A
NM_001281493.2:c.2266+1G>A (MSH6)	NP_001268422.1:n.2266+1G>A
NM_001281494.2:c.2266+1G>A (MSH6)	NP_001268423.1:n.2266+1G>A