Canonical Allele Identifier: CA913187977

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 924505
• ClinVar RCV Id: RCV001185871
• dbSNP Id: rs1669775885

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803694_47803695insA , CM000664.2:g.47803694_47803695insA	GRCh38
NC_000002.11:g.48030833_48030834insA , CM000664.1:g.48030833_48030834insA	GRCh37
NC_000002.10:g.47884337_47884338insA	NCBI36
NG_007111.1:g.25548_25549insA , LRG_219:g.25548_25549insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3141+9_3141+10insA (MSH6)	ENSP00000406248.2:n.3141+9_3141+10insA
ENST00000420813.6:c.3141+9_3141+10insA (MSH6)	ENSP00000390382.2:n.3141+9_3141+10insA
ENST00000455383.6:c.3141+9_3141+10insA (MSH6)	ENSP00000397484.2:n.3141+9_3141+10insA
ENST00000700004.2:c.3173-1924_3173-1923insA (MSH6)	ENSP00000514752.2:n.3173-1924_3173-1923in...
ENST00000699999.1:n.3522+9_3522+10insA (MSH6)
ENST00000700000.1:c.1872+9_1872+10insA (MSH6)	ENSP00000514749.1:n.1872+9_1872+10insA
ENST00000700002.1:c.3444+9_3444+10insA (MSH6)	ENSP00000514750.1:n.3444+9_3444+10insA
ENST00000700003.1:c.893+9_893+10insA (MSH6)	ENSP00000514751.1:n.893+9_893+10insA
ENST00000700004.1:c.2330-1924_2330-1923insA (MSH6)	ENSP00000514752.1:n.2330-1924_2330-1923in...
ENST00000700005.1:n.2289+9_2289+10insA (MSH6)
ENST00000700006.1:n.2295_2296insA (MSH6)
ENST00000700007.1:n.1443+9_1443+10insA (MSH6)
ENST00000700008.1:n.1017+9_1017+10insA (MSH6)
ENST00000700009.1:n.1016+9_1016+10insA (MSH6)
ENST00000700010.1:n.847+9_847+10insA (MSH6)
ENST00000700011.1:n.927_928insA (MSH6)
ENST00000234420.11:c.3438+9_3438+10insA (MSH6) MANE Select	ENSP00000234420.5:n.3438+9_3438+10insA
ENST00000540021.6:c.3048+9_3048+10insA (MSH6)	ENSP00000446475.1:n.3048+9_3048+10insA
ENST00000652107.1:c.3141+9_3141+10insA (MSH6)	ENSP00000498629.1:n.3141+9_3141+10insA
ENST00000673637.1:c.3141+9_3141+10insA (MSH6)	ENSP00000501310.1:n.3141+9_3141+10insA
ENST00000234420.9:c.3438+9_3438+10insA (MSH6)	ENSP00000234420.4:n.3438+9_3438+10insA
ENST00000405808.5:c.169+4500_169+4501insT (FBXO11)	ENSP00000385127.1:n.169+4500_169+4501insT...
ENST00000434234.5:c.*124+4299_*124+4300insT (FBXO11)	ENSP00000402692.1:n.*124+4299_*124+4300in...
ENST00000445503.5:c.*2785+9_*2785+10insA (MSH6)	ENSP00000405294.1:n.*2785+9_*2785+10insA
ENST00000538136.1:c.2532+9_2532+10insA (MSH6)	ENSP00000438580.1:n.2532+9_2532+10insA
ENST00000540021.5:c.3048+9_3048+10insA (MSH6)	ENSP00000446475.1:n.3048+9_3048+10insA
ENST00000614496.4:c.2532+9_2532+10insA (MSH6)	ENSP00000477844.1:n.2532+9_2532+10insA
ENST00000622629.4:c.334+16_334+17insA (MSH6)	ENSP00000482078.1:n.334+16_334+17insA
NM_000179.2:c.3438+9_3438+10insA , LRG_219t1:c.3438+9_3438+10insA (MSH6)	NP_000170.1:n.3438+9_3438+10insA
NM_001281492.1:c.3048+9_3048+10insA (MSH6)	NP_001268421.1:n.3048+9_3048+10insA
NM_001281493.1:c.2532+9_2532+10insA (MSH6)	NP_001268422.1:n.2532+9_2532+10insA
NM_001281494.1:c.2532+9_2532+10insA (MSH6)	NP_001268423.1:n.2532+9_2532+10insA
XM_005264271.1:c.3141+9_3141+10insA (MSH6)	XP_005264328.1:n.3141+9_3141+10insA
XM_011532798.1:c.3255+9_3255+10insA (MSH6)	XP_011531100.1:n.3255+9_3255+10insA
XM_011532799.1:c.3141+9_3141+10insA (MSH6)	XP_011531101.1:n.3141+9_3141+10insA
XM_011532800.1:c.3141+9_3141+10insA (MSH6)	XP_011531102.1:n.3141+9_3141+10insA
XM_024452819.1:c.3438+9_3438+10insA (MSH6)	XP_024308587.1:n.3438+9_3438+10insA
XM_024452820.1:c.3255+9_3255+10insA (MSH6)	XP_024308588.1:n.3255+9_3255+10insA
XM_024452821.1:c.3141+9_3141+10insA (MSH6)	XP_024308589.1:n.3141+9_3141+10insA
XM_024452822.1:c.2532+9_2532+10insA (MSH6)	XP_024308590.1:n.2532+9_2532+10insA
NM_000179.3:c.3438+9_3438+10insA (MSH6) MANE Select	NP_000170.1:n.3438+9_3438+10insA
NM_001281492.2:c.3048+9_3048+10insA (MSH6)	NP_001268421.1:n.3048+9_3048+10insA
NM_001281493.2:c.2532+9_2532+10insA (MSH6)	NP_001268422.1:n.2532+9_2532+10insA
NM_001281494.2:c.2532+9_2532+10insA (MSH6)	NP_001268423.1:n.2532+9_2532+10insA