Canonical Allele Identifier: CA346760238

Gene: MSH6 FBXO11

Linked Data

• MyVariant Identifiers: chr2:g.48032145G>A (hg19) ; chr2:g.47805006G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805006G>A , CM000664.2:g.47805006G>A	GRCh38
NC_000002.11:g.48032145G>A , CM000664.1:g.48032145G>A	GRCh37
NC_000002.10:g.47885649G>A	NCBI36
NG_007111.1:g.26860G>A , LRG_219:g.26860G>A
NG_008397.1:g.105670C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3238G>A (MSH6)	ENSP00000406248.2:p.Ala1080Thr
ENST00000420813.6:c.3238G>A (MSH6)	ENSP00000390382.2:p.Ala1080Thr
ENST00000455383.6:c.3238G>A (MSH6)	ENSP00000397484.2:p.Ala1080Thr
ENST00000700004.2:c.3173-612G>A (MSH6)	ENSP00000514752.2:n.3173-612G>A
ENST00000699999.1:n.3619G>A (MSH6)
ENST00000700000.1:c.1969G>A (MSH6)	ENSP00000514749.1:p.Ala657Thr
ENST00000700002.1:c.3541G>A (MSH6)	ENSP00000514750.1:p.Ala1181Thr
ENST00000700003.1:c.990G>A (MSH6)	ENSP00000514751.1:n.990G>A
ENST00000700004.1:c.2330-612G>A (MSH6)	ENSP00000514752.1:n.2330-612G>A
ENST00000700005.1:n.2386G>A (MSH6)
ENST00000700006.1:n.3607G>A (MSH6)
ENST00000700007.1:n.1540G>A (MSH6)
ENST00000700008.1:n.1114G>A (MSH6)
ENST00000700009.1:n.1113G>A (MSH6)
ENST00000700010.1:n.944G>A (MSH6)
ENST00000700011.1:n.2239G>A (MSH6)
ENST00000234420.11:c.3535G>A (MSH6) MANE Select	ENSP00000234420.5:p.Ala1179Thr
ENST00000540021.6:c.3145G>A (MSH6)	ENSP00000446475.1:p.Ala1049Thr
ENST00000652107.1:c.3238G>A (MSH6)	ENSP00000498629.1:p.Ala1080Thr
ENST00000673637.1:c.3238G>A (MSH6)	ENSP00000501310.1:p.Ala1080Thr
ENST00000234420.9:c.3535G>A (MSH6)	ENSP00000234420.4:p.Ala1179Thr
ENST00000405808.5:c.169+3189C>T (FBXO11)	ENSP00000385127.1:n.169+3189C>T
ENST00000434234.5:c.*124+2988C>T (FBXO11)	ENSP00000402692.1:n.*124+2988C>T
ENST00000445503.5:c.*2882G>A (MSH6)	ENSP00000405294.1:n.*2882G>A
ENST00000538136.1:c.2629G>A (MSH6)	ENSP00000438580.1:p.Ala877Thr
ENST00000540021.5:c.3145G>A (MSH6)	ENSP00000446475.1:p.Ala1049Thr
ENST00000614496.4:c.2629G>A (MSH6)	ENSP00000477844.1:p.Ala877Thr
ENST00000622629.4:c.439G>A (MSH6)	ENSP00000482078.1:p.Ala147Thr
NM_000179.2:c.3535G>A , LRG_219t1:c.3535G>A (MSH6)	NP_000170.1:p.Ala1179Thr
NM_001281492.1:c.3145G>A (MSH6)	NP_001268421.1:p.Ala1049Thr
NM_001281493.1:c.2629G>A (MSH6)	NP_001268422.1:p.Ala877Thr
NM_001281494.1:c.2629G>A (MSH6)	NP_001268423.1:p.Ala877Thr
XM_005264271.1:c.3238G>A (MSH6)	XP_005264328.1:p.Ala1080Thr
XM_011532798.1:c.3352G>A (MSH6)	XP_011531100.1:p.Ala1118Thr
XM_011532799.1:c.3238G>A (MSH6)	XP_011531101.1:p.Ala1080Thr
XM_011532800.1:c.3238G>A (MSH6)	XP_011531102.1:p.Ala1080Thr
XM_024452819.1:c.3535G>A (MSH6)	XP_024308587.1:p.Ala1179Thr
XM_024452820.1:c.3352G>A (MSH6)	XP_024308588.1:p.Ala1118Thr
XM_024452821.1:c.3238G>A (MSH6)	XP_024308589.1:p.Ala1080Thr
XM_024452822.1:c.2629G>A (MSH6)	XP_024308590.1:p.Ala877Thr
NM_000179.3:c.3535G>A (MSH6) MANE Select	NP_000170.1:p.Ala1179Thr
NM_001281492.2:c.3145G>A (MSH6)	NP_001268421.1:p.Ala1049Thr
NM_001281493.2:c.2629G>A (MSH6)	NP_001268422.1:p.Ala877Thr
NM_001281494.2:c.2629G>A (MSH6)	NP_001268423.1:p.Ala877Thr