Canonical Allele Identifier: CA769464099

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1218941627
• MyVariant Identifiers: chr2:g.48032536_48032537insTAAC (hg19) ; chr2:g.47805397_47805398insTAAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805399_47805402dup , CM000664.2:g.47805399_47805402dup	GRCh38
NC_000002.11:g.48032538_48032541dup , CM000664.1:g.48032538_48032541dup	GRCh37
NC_000002.10:g.47886042_47886045dup	NCBI36
NG_007111.1:g.27253_27256dup , LRG_219:g.27253_27256dup
NG_008397.1:g.105275_105278dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3260-219_3260-216dup (MSH6)	ENSP00000406248.2:n.3260-219_3260-216dup
ENST00000420813.6:c.3260-219_3260-216dup (MSH6)	ENSP00000390382.2:n.3260-219_3260-216dup
ENST00000455383.6:c.3260-219_3260-216dup (MSH6)	ENSP00000397484.2:n.3260-219_3260-216dup
ENST00000700004.2:c.3173-219_3173-216dup (MSH6)	ENSP00000514752.2:n.3173-219_3173-216dup
ENST00000699999.1:n.4012_4015dup (MSH6)
ENST00000700000.1:c.1991-219_1991-216dup (MSH6)	ENSP00000514749.1:n.1991-219_1991-216dup
ENST00000700002.1:c.3563-219_3563-216dup (MSH6)	ENSP00000514750.1:n.3563-219_3563-216dup
ENST00000700003.1:c.1012-219_1012-216dup (MSH6)	ENSP00000514751.1:n.1012-219_1012-216dup
ENST00000700004.1:c.2330-219_2330-216dup (MSH6)	ENSP00000514752.1:n.2330-219_2330-216dup
ENST00000700005.1:n.2408-219_2408-216dup (MSH6)
ENST00000700006.1:n.4000_4003dup (MSH6)
ENST00000700007.1:n.1933_1936dup (MSH6)
ENST00000700008.1:n.1507_1510dup (MSH6)
ENST00000700009.1:n.1506_1509dup (MSH6)
ENST00000700010.1:n.966-219_966-216dup (MSH6)
ENST00000700011.1:n.2632_2635dup (MSH6)
ENST00000234420.11:c.3557-219_3557-216dup (MSH6) MANE Select	ENSP00000234420.5:n.3557-219_3557-216dup
ENST00000540021.6:c.3167-219_3167-216dup (MSH6)	ENSP00000446475.1:n.3167-219_3167-216dup
ENST00000652107.1:c.3260-219_3260-216dup (MSH6)	ENSP00000498629.1:n.3260-219_3260-216dup
ENST00000673637.1:c.3260-219_3260-216dup (MSH6)	ENSP00000501310.1:n.3260-219_3260-216dup
ENST00000234420.9:c.3557-219_3557-216dup (MSH6)	ENSP00000234420.4:n.3557-219_3557-216dup
ENST00000405808.5:c.169+2794_169+2797dup (FBXO11)	ENSP00000385127.1:n.169+2794_169+2797dup
ENST00000434234.5:c.*124+2593_*124+2596dup (FBXO11)	ENSP00000402692.1:n.*124+2593_*124+2596dup
ENST00000445503.5:c.*2904-219_*2904-216dup (MSH6)	ENSP00000405294.1:n.*2904-219_*2904-216dup
ENST00000538136.1:c.2651-219_2651-216dup (MSH6)	ENSP00000438580.1:n.2651-219_2651-216dup
ENST00000540021.5:c.3167-219_3167-216dup (MSH6)	ENSP00000446475.1:n.3167-219_3167-216dup
ENST00000614496.4:c.2651-219_2651-216dup (MSH6)	ENSP00000477844.1:n.2651-219_2651-216dup
ENST00000622629.4:c.461-219_461-216dup (MSH6)	ENSP00000482078.1:n.461-219_461-216dup
NM_000179.2:c.3557-219_3557-216dup , LRG_219t1:c.3557-219_3557-216dup (MSH6)	NP_000170.1:n.3557-219_3557-216dup
NM_001281492.1:c.3167-219_3167-216dup (MSH6)	NP_001268421.1:n.3167-219_3167-216dup
NM_001281493.1:c.2651-219_2651-216dup (MSH6)	NP_001268422.1:n.2651-219_2651-216dup
NM_001281494.1:c.2651-219_2651-216dup (MSH6)	NP_001268423.1:n.2651-219_2651-216dup
XM_005264271.1:c.3260-219_3260-216dup (MSH6)	XP_005264328.1:n.3260-219_3260-216dup
XM_011532798.1:c.3374-219_3374-216dup (MSH6)	XP_011531100.1:n.3374-219_3374-216dup
XM_011532799.1:c.3260-219_3260-216dup (MSH6)	XP_011531101.1:n.3260-219_3260-216dup
XM_011532800.1:c.3260-219_3260-216dup (MSH6)	XP_011531102.1:n.3260-219_3260-216dup
XM_024452819.1:c.3557-219_3557-216dup (MSH6)	XP_024308587.1:n.3557-219_3557-216dup
XM_024452820.1:c.3374-219_3374-216dup (MSH6)	XP_024308588.1:n.3374-219_3374-216dup
XM_024452821.1:c.3260-219_3260-216dup (MSH6)	XP_024308589.1:n.3260-219_3260-216dup
XM_024452822.1:c.2651-219_2651-216dup (MSH6)	XP_024308590.1:n.2651-219_2651-216dup
NM_000179.3:c.3557-219_3557-216dup (MSH6) MANE Select	NP_000170.1:n.3557-219_3557-216dup
NM_001281492.2:c.3167-219_3167-216dup (MSH6)	NP_001268421.1:n.3167-219_3167-216dup
NM_001281493.2:c.2651-219_2651-216dup (MSH6)	NP_001268422.1:n.2651-219_2651-216dup
NM_001281494.2:c.2651-219_2651-216dup (MSH6)	NP_001268423.1:n.2651-219_2651-216dup