Canonical Allele Identifier: CA1030294967

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1669946836
• gnomAD v3: 2-47805569-A-AT
• gnomAD v4: 2-47805569-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805569_47805570insT , CM000664.2:g.47805569_47805570insT	GRCh38
NC_000002.11:g.48032708_48032709insT , CM000664.1:g.48032708_48032709insT	GRCh37
NC_000002.10:g.47886212_47886213insT	NCBI36
NG_007111.1:g.27423_27424insT , LRG_219:g.27423_27424insT
NG_008397.1:g.105106_105107insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3260-49_3260-48insT (MSH6)	ENSP00000406248.2:n.3260-49_3260-48insT
ENST00000420813.6:c.3260-49_3260-48insT (MSH6)	ENSP00000390382.2:n.3260-49_3260-48insT
ENST00000455383.6:c.3260-49_3260-48insT (MSH6)	ENSP00000397484.2:n.3260-49_3260-48insT
ENST00000700004.2:c.3173-49_3173-48insT (MSH6)	ENSP00000514752.2:n.3173-49_3173-48insT
ENST00000699999.1:n.4182_4183insT (MSH6)
ENST00000700000.1:c.1991-49_1991-48insT (MSH6)	ENSP00000514749.1:n.1991-49_1991-48insT
ENST00000700002.1:c.3563-49_3563-48insT (MSH6)	ENSP00000514750.1:n.3563-49_3563-48insT
ENST00000700003.1:c.1012-49_1012-48insT (MSH6)	ENSP00000514751.1:n.1012-49_1012-48insT
ENST00000700004.1:c.2330-49_2330-48insT (MSH6)	ENSP00000514752.1:n.2330-49_2330-48insT
ENST00000700005.1:n.2408-49_2408-48insT (MSH6)
ENST00000700006.1:n.4170_4171insT (MSH6)
ENST00000700007.1:n.2103_2104insT (MSH6)
ENST00000700008.1:n.1677_1678insT (MSH6)
ENST00000700009.1:n.1676_1677insT (MSH6)
ENST00000700010.1:n.966-49_966-48insT (MSH6)
ENST00000700011.1:n.2802_2803insT (MSH6)
ENST00000234420.11:c.3557-49_3557-48insT (MSH6) MANE Select	ENSP00000234420.5:n.3557-49_3557-48insT
ENST00000540021.6:c.3167-49_3167-48insT (MSH6)	ENSP00000446475.1:n.3167-49_3167-48insT
ENST00000652107.1:c.3260-49_3260-48insT (MSH6)	ENSP00000498629.1:n.3260-49_3260-48insT
ENST00000673637.1:c.3260-49_3260-48insT (MSH6)	ENSP00000501310.1:n.3260-49_3260-48insT
ENST00000234420.9:c.3557-49_3557-48insT (MSH6)	ENSP00000234420.4:n.3557-49_3557-48insT
ENST00000405808.5:c.169+2625_169+2626insA (FBXO11)	ENSP00000385127.1:n.169+2625_169+2626insA...
ENST00000434234.5:c.*124+2424_*124+2425insA (FBXO11)	ENSP00000402692.1:n.*124+2424_*124+2425in...
ENST00000445503.5:c.*2904-49_*2904-48insT (MSH6)	ENSP00000405294.1:n.*2904-49_*2904-48insT...
ENST00000538136.1:c.2651-49_2651-48insT (MSH6)	ENSP00000438580.1:n.2651-49_2651-48insT
ENST00000540021.5:c.3167-49_3167-48insT (MSH6)	ENSP00000446475.1:n.3167-49_3167-48insT
ENST00000614496.4:c.2651-49_2651-48insT (MSH6)	ENSP00000477844.1:n.2651-49_2651-48insT
ENST00000622629.4:c.461-49_461-48insT (MSH6)	ENSP00000482078.1:n.461-49_461-48insT
NM_000179.2:c.3557-49_3557-48insT , LRG_219t1:c.3557-49_3557-48insT (MSH6)	NP_000170.1:n.3557-49_3557-48insT
NM_001281492.1:c.3167-49_3167-48insT (MSH6)	NP_001268421.1:n.3167-49_3167-48insT
NM_001281493.1:c.2651-49_2651-48insT (MSH6)	NP_001268422.1:n.2651-49_2651-48insT
NM_001281494.1:c.2651-49_2651-48insT (MSH6)	NP_001268423.1:n.2651-49_2651-48insT
XM_005264271.1:c.3260-49_3260-48insT (MSH6)	XP_005264328.1:n.3260-49_3260-48insT
XM_011532798.1:c.3374-49_3374-48insT (MSH6)	XP_011531100.1:n.3374-49_3374-48insT
XM_011532799.1:c.3260-49_3260-48insT (MSH6)	XP_011531101.1:n.3260-49_3260-48insT
XM_011532800.1:c.3260-49_3260-48insT (MSH6)	XP_011531102.1:n.3260-49_3260-48insT
XM_024452819.1:c.3557-49_3557-48insT (MSH6)	XP_024308587.1:n.3557-49_3557-48insT
XM_024452820.1:c.3374-49_3374-48insT (MSH6)	XP_024308588.1:n.3374-49_3374-48insT
XM_024452821.1:c.3260-49_3260-48insT (MSH6)	XP_024308589.1:n.3260-49_3260-48insT
XM_024452822.1:c.2651-49_2651-48insT (MSH6)	XP_024308590.1:n.2651-49_2651-48insT
NM_000179.3:c.3557-49_3557-48insT (MSH6) MANE Select	NP_000170.1:n.3557-49_3557-48insT
NM_001281492.2:c.3167-49_3167-48insT (MSH6)	NP_001268421.1:n.3167-49_3167-48insT
NM_001281493.2:c.2651-49_2651-48insT (MSH6)	NP_001268422.1:n.2651-49_2651-48insT
NM_001281494.2:c.2651-49_2651-48insT (MSH6)	NP_001268423.1:n.2651-49_2651-48insT