Canonical Allele Identifier: CA769464044

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1288918367
• MyVariant Identifiers: chr2:g.48032482_48032483insTAA (hg19) ; chr2:g.47805343_47805344insTAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805345_47805347dup , CM000664.2:g.47805345_47805347dup	GRCh38
NC_000002.11:g.48032484_48032486dup , CM000664.1:g.48032484_48032486dup	GRCh37
NC_000002.10:g.47885988_47885990dup	NCBI36
NG_007111.1:g.27199_27201dup , LRG_219:g.27199_27201dup
NG_008397.1:g.105330_105332dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3260-273_3260-271dup (MSH6)	ENSP00000406248.2:n.3260-273_3260-271dup
ENST00000420813.6:c.3260-273_3260-271dup (MSH6)	ENSP00000390382.2:n.3260-273_3260-271dup
ENST00000455383.6:c.3260-273_3260-271dup (MSH6)	ENSP00000397484.2:n.3260-273_3260-271dup
ENST00000700004.2:c.3173-273_3173-271dup (MSH6)	ENSP00000514752.2:n.3173-273_3173-271dup
ENST00000699999.1:n.3958_3960dup (MSH6)
ENST00000700000.1:c.1991-273_1991-271dup (MSH6)	ENSP00000514749.1:n.1991-273_1991-271dup
ENST00000700002.1:c.3563-273_3563-271dup (MSH6)	ENSP00000514750.1:n.3563-273_3563-271dup
ENST00000700003.1:c.1012-273_1012-271dup (MSH6)	ENSP00000514751.1:n.1012-273_1012-271dup
ENST00000700004.1:c.2330-273_2330-271dup (MSH6)	ENSP00000514752.1:n.2330-273_2330-271dup
ENST00000700005.1:n.2408-273_2408-271dup (MSH6)
ENST00000700006.1:n.3946_3948dup (MSH6)
ENST00000700007.1:n.1879_1881dup (MSH6)
ENST00000700008.1:n.1453_1455dup (MSH6)
ENST00000700009.1:n.1452_1454dup (MSH6)
ENST00000700010.1:n.966-273_966-271dup (MSH6)
ENST00000700011.1:n.2578_2580dup (MSH6)
ENST00000234420.11:c.3557-273_3557-271dup (MSH6) MANE Select	ENSP00000234420.5:n.3557-273_3557-271dup
ENST00000540021.6:c.3167-273_3167-271dup (MSH6)	ENSP00000446475.1:n.3167-273_3167-271dup
ENST00000652107.1:c.3260-273_3260-271dup (MSH6)	ENSP00000498629.1:n.3260-273_3260-271dup
ENST00000673637.1:c.3260-273_3260-271dup (MSH6)	ENSP00000501310.1:n.3260-273_3260-271dup
ENST00000234420.9:c.3557-273_3557-271dup (MSH6)	ENSP00000234420.4:n.3557-273_3557-271dup
ENST00000405808.5:c.169+2849_169+2851dup (FBXO11)	ENSP00000385127.1:n.169+2849_169+2851dup
ENST00000434234.5:c.*124+2648_*124+2650dup (FBXO11)	ENSP00000402692.1:n.*124+2648_*124+2650dup
ENST00000445503.5:c.*2904-273_*2904-271dup (MSH6)	ENSP00000405294.1:n.*2904-273_*2904-271dup
ENST00000538136.1:c.2651-273_2651-271dup (MSH6)	ENSP00000438580.1:n.2651-273_2651-271dup
ENST00000540021.5:c.3167-273_3167-271dup (MSH6)	ENSP00000446475.1:n.3167-273_3167-271dup
ENST00000614496.4:c.2651-273_2651-271dup (MSH6)	ENSP00000477844.1:n.2651-273_2651-271dup
ENST00000622629.4:c.461-273_461-271dup (MSH6)	ENSP00000482078.1:n.461-273_461-271dup
NM_000179.2:c.3557-273_3557-271dup , LRG_219t1:c.3557-273_3557-271dup (MSH6)	NP_000170.1:n.3557-273_3557-271dup
NM_001281492.1:c.3167-273_3167-271dup (MSH6)	NP_001268421.1:n.3167-273_3167-271dup
NM_001281493.1:c.2651-273_2651-271dup (MSH6)	NP_001268422.1:n.2651-273_2651-271dup
NM_001281494.1:c.2651-273_2651-271dup (MSH6)	NP_001268423.1:n.2651-273_2651-271dup
XM_005264271.1:c.3260-273_3260-271dup (MSH6)	XP_005264328.1:n.3260-273_3260-271dup
XM_011532798.1:c.3374-273_3374-271dup (MSH6)	XP_011531100.1:n.3374-273_3374-271dup
XM_011532799.1:c.3260-273_3260-271dup (MSH6)	XP_011531101.1:n.3260-273_3260-271dup
XM_011532800.1:c.3260-273_3260-271dup (MSH6)	XP_011531102.1:n.3260-273_3260-271dup
XM_024452819.1:c.3557-273_3557-271dup (MSH6)	XP_024308587.1:n.3557-273_3557-271dup
XM_024452820.1:c.3374-273_3374-271dup (MSH6)	XP_024308588.1:n.3374-273_3374-271dup
XM_024452821.1:c.3260-273_3260-271dup (MSH6)	XP_024308589.1:n.3260-273_3260-271dup
XM_024452822.1:c.2651-273_2651-271dup (MSH6)	XP_024308590.1:n.2651-273_2651-271dup
NM_000179.3:c.3557-273_3557-271dup (MSH6) MANE Select	NP_000170.1:n.3557-273_3557-271dup
NM_001281492.2:c.3167-273_3167-271dup (MSH6)	NP_001268421.1:n.3167-273_3167-271dup
NM_001281493.2:c.2651-273_2651-271dup (MSH6)	NP_001268422.1:n.2651-273_2651-271dup
NM_001281494.2:c.2651-273_2651-271dup (MSH6)	NP_001268423.1:n.2651-273_2651-271dup