Canonical Allele Identifier: CA2496053215

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs1669916533

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805317_47805321dup , CM000664.2:g.47805317_47805321dup	GRCh38
NC_000002.11:g.48032456_48032460dup , CM000664.1:g.48032456_48032460dup	GRCh37
NC_000002.10:g.47885960_47885964dup	NCBI36
NG_007111.1:g.27171_27175dup , LRG_219:g.27171_27175dup
NG_008397.1:g.105356_105360dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3259+290_3259+294dup (MSH6)	ENSP00000406248.2:n.3259+290_3259+294dup
ENST00000420813.6:c.3259+290_3259+294dup (MSH6)	ENSP00000390382.2:n.3259+290_3259+294dup
ENST00000455383.6:c.3259+290_3259+294dup (MSH6)	ENSP00000397484.2:n.3259+290_3259+294dup
ENST00000700004.2:c.3173-301_3173-297dup (MSH6)	ENSP00000514752.2:n.3173-301_3173-297dup
ENST00000699999.1:n.3930_3934dup (MSH6)
ENST00000700000.1:c.1990+290_1990+294dup (MSH6)	ENSP00000514749.1:n.1990+290_1990+294dup
ENST00000700002.1:c.3562+290_3562+294dup (MSH6)	ENSP00000514750.1:n.3562+290_3562+294dup
ENST00000700003.1:c.1011+290_1011+294dup (MSH6)	ENSP00000514751.1:n.1011+290_1011+294dup
ENST00000700004.1:c.2330-301_2330-297dup (MSH6)	ENSP00000514752.1:n.2330-301_2330-297dup
ENST00000700005.1:n.2407+290_2407+294dup (MSH6)
ENST00000700006.1:n.3918_3922dup (MSH6)
ENST00000700007.1:n.1851_1855dup (MSH6)
ENST00000700008.1:n.1425_1429dup (MSH6)
ENST00000700009.1:n.1424_1428dup (MSH6)
ENST00000700010.1:n.965+290_965+294dup (MSH6)
ENST00000700011.1:n.2550_2554dup (MSH6)
ENST00000234420.11:c.3556+290_3556+294dup (MSH6) MANE Select	ENSP00000234420.5:n.3556+290_3556+294dup
ENST00000540021.6:c.3166+290_3166+294dup (MSH6)	ENSP00000446475.1:n.3166+290_3166+294dup
ENST00000652107.1:c.3259+290_3259+294dup (MSH6)	ENSP00000498629.1:n.3259+290_3259+294dup
ENST00000673637.1:c.3259+290_3259+294dup (MSH6)	ENSP00000501310.1:n.3259+290_3259+294dup
ENST00000234420.9:c.3556+290_3556+294dup (MSH6)	ENSP00000234420.4:n.3556+290_3556+294dup
ENST00000405808.5:c.169+2875_169+2879dup (FBXO11)	ENSP00000385127.1:n.169+2875_169+2879dup
ENST00000434234.5:c.*124+2674_*124+2678dup (FBXO11)	ENSP00000402692.1:n.*124+2674_*124+2678dup
ENST00000445503.5:c.*2903+290_*2903+294dup (MSH6)	ENSP00000405294.1:n.*2903+290_*2903+294dup
ENST00000538136.1:c.2650+290_2650+294dup (MSH6)	ENSP00000438580.1:n.2650+290_2650+294dup
ENST00000540021.5:c.3166+290_3166+294dup (MSH6)	ENSP00000446475.1:n.3166+290_3166+294dup
ENST00000614496.4:c.2650+290_2650+294dup (MSH6)	ENSP00000477844.1:n.2650+290_2650+294dup
ENST00000622629.4:c.460+290_460+294dup (MSH6)	ENSP00000482078.1:n.460+290_460+294dup
NM_000179.2:c.3556+290_3556+294dup , LRG_219t1:c.3556+290_3556+294dup (MSH6)	NP_000170.1:n.3556+290_3556+294dup
NM_001281492.1:c.3166+290_3166+294dup (MSH6)	NP_001268421.1:n.3166+290_3166+294dup
NM_001281493.1:c.2650+290_2650+294dup (MSH6)	NP_001268422.1:n.2650+290_2650+294dup
NM_001281494.1:c.2650+290_2650+294dup (MSH6)	NP_001268423.1:n.2650+290_2650+294dup
XM_005264271.1:c.3259+290_3259+294dup (MSH6)	XP_005264328.1:n.3259+290_3259+294dup
XM_011532798.1:c.3373+290_3373+294dup (MSH6)	XP_011531100.1:n.3373+290_3373+294dup
XM_011532799.1:c.3259+290_3259+294dup (MSH6)	XP_011531101.1:n.3259+290_3259+294dup
XM_011532800.1:c.3259+290_3259+294dup (MSH6)	XP_011531102.1:n.3259+290_3259+294dup
XM_024452819.1:c.3556+290_3556+294dup (MSH6)	XP_024308587.1:n.3556+290_3556+294dup
XM_024452820.1:c.3373+290_3373+294dup (MSH6)	XP_024308588.1:n.3373+290_3373+294dup
XM_024452821.1:c.3259+290_3259+294dup (MSH6)	XP_024308589.1:n.3259+290_3259+294dup
XM_024452822.1:c.2650+290_2650+294dup (MSH6)	XP_024308590.1:n.2650+290_2650+294dup
NM_000179.3:c.3556+290_3556+294dup (MSH6) MANE Select	NP_000170.1:n.3556+290_3556+294dup
NM_001281492.2:c.3166+290_3166+294dup (MSH6)	NP_001268421.1:n.3166+290_3166+294dup
NM_001281493.2:c.2650+290_2650+294dup (MSH6)	NP_001268422.1:n.2650+290_2650+294dup
NM_001281494.2:c.2650+290_2650+294dup (MSH6)	NP_001268423.1:n.2650+290_2650+294dup