Canonical Allele Identifier: CA2658965896

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47805048-T-TTAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805050_47805053dup , CM000664.2:g.47805050_47805053dup	GRCh38
NC_000002.11:g.48032189_48032192dup , CM000664.1:g.48032189_48032192dup	GRCh37
NC_000002.10:g.47885693_47885696dup	NCBI36
NG_007111.1:g.26904_26907dup , LRG_219:g.26904_26907dup
NG_008397.1:g.105624_105627dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3259+23_3259+26dup (MSH6)	ENSP00000406248.2:n.3259+23_3259+26dup
ENST00000420813.6:c.3259+23_3259+26dup (MSH6)	ENSP00000390382.2:n.3259+23_3259+26dup
ENST00000455383.6:c.3259+23_3259+26dup (MSH6)	ENSP00000397484.2:n.3259+23_3259+26dup
ENST00000700004.2:c.3173-568_3173-565dup (MSH6)	ENSP00000514752.2:n.3173-568_3173-565dup
ENST00000699999.1:n.3663_3666dup (MSH6)
ENST00000700000.1:c.1990+23_1990+26dup (MSH6)	ENSP00000514749.1:n.1990+23_1990+26dup
ENST00000700002.1:c.3562+23_3562+26dup (MSH6)	ENSP00000514750.1:n.3562+23_3562+26dup
ENST00000700003.1:c.1011+23_1011+26dup (MSH6)	ENSP00000514751.1:n.1011+23_1011+26dup
ENST00000700004.1:c.2330-568_2330-565dup (MSH6)	ENSP00000514752.1:n.2330-568_2330-565dup
ENST00000700005.1:n.2407+23_2407+26dup (MSH6)
ENST00000700006.1:n.3651_3654dup (MSH6)
ENST00000700007.1:n.1584_1587dup (MSH6)
ENST00000700008.1:n.1158_1161dup (MSH6)
ENST00000700009.1:n.1157_1160dup (MSH6)
ENST00000700010.1:n.965+23_965+26dup (MSH6)
ENST00000700011.1:n.2283_2286dup (MSH6)
ENST00000234420.11:c.3556+23_3556+26dup (MSH6) MANE Select	ENSP00000234420.5:n.3556+23_3556+26dup
ENST00000540021.6:c.3166+23_3166+26dup (MSH6)	ENSP00000446475.1:n.3166+23_3166+26dup
ENST00000652107.1:c.3259+23_3259+26dup (MSH6)	ENSP00000498629.1:n.3259+23_3259+26dup
ENST00000673637.1:c.3259+23_3259+26dup (MSH6)	ENSP00000501310.1:n.3259+23_3259+26dup
ENST00000234420.9:c.3556+23_3556+26dup (MSH6)	ENSP00000234420.4:n.3556+23_3556+26dup
ENST00000405808.5:c.169+3143_169+3146dup (FBXO11)	ENSP00000385127.1:n.169+3143_169+3146dup
ENST00000434234.5:c.*124+2942_*124+2945dup (FBXO11)	ENSP00000402692.1:n.*124+2942_*124+2945dup
ENST00000445503.5:c.*2903+23_*2903+26dup (MSH6)	ENSP00000405294.1:n.*2903+23_*2903+26dup
ENST00000538136.1:c.2650+23_2650+26dup (MSH6)	ENSP00000438580.1:n.2650+23_2650+26dup
ENST00000540021.5:c.3166+23_3166+26dup (MSH6)	ENSP00000446475.1:n.3166+23_3166+26dup
ENST00000614496.4:c.2650+23_2650+26dup (MSH6)	ENSP00000477844.1:n.2650+23_2650+26dup
ENST00000622629.4:c.460+23_460+26dup (MSH6)	ENSP00000482078.1:n.460+23_460+26dup
NM_000179.2:c.3556+23_3556+26dup , LRG_219t1:c.3556+23_3556+26dup (MSH6)	NP_000170.1:n.3556+23_3556+26dup
NM_001281492.1:c.3166+23_3166+26dup (MSH6)	NP_001268421.1:n.3166+23_3166+26dup
NM_001281493.1:c.2650+23_2650+26dup (MSH6)	NP_001268422.1:n.2650+23_2650+26dup
NM_001281494.1:c.2650+23_2650+26dup (MSH6)	NP_001268423.1:n.2650+23_2650+26dup
XM_005264271.1:c.3259+23_3259+26dup (MSH6)	XP_005264328.1:n.3259+23_3259+26dup
XM_011532798.1:c.3373+23_3373+26dup (MSH6)	XP_011531100.1:n.3373+23_3373+26dup
XM_011532799.1:c.3259+23_3259+26dup (MSH6)	XP_011531101.1:n.3259+23_3259+26dup
XM_011532800.1:c.3259+23_3259+26dup (MSH6)	XP_011531102.1:n.3259+23_3259+26dup
XM_024452819.1:c.3556+23_3556+26dup (MSH6)	XP_024308587.1:n.3556+23_3556+26dup
XM_024452820.1:c.3373+23_3373+26dup (MSH6)	XP_024308588.1:n.3373+23_3373+26dup
XM_024452821.1:c.3259+23_3259+26dup (MSH6)	XP_024308589.1:n.3259+23_3259+26dup
XM_024452822.1:c.2650+23_2650+26dup (MSH6)	XP_024308590.1:n.2650+23_2650+26dup
NM_000179.3:c.3556+23_3556+26dup (MSH6) MANE Select	NP_000170.1:n.3556+23_3556+26dup
NM_001281492.2:c.3166+23_3166+26dup (MSH6)	NP_001268421.1:n.3166+23_3166+26dup
NM_001281493.2:c.2650+23_2650+26dup (MSH6)	NP_001268422.1:n.2650+23_2650+26dup
NM_001281494.2:c.2650+23_2650+26dup (MSH6)	NP_001268423.1:n.2650+23_2650+26dup