Canonical Allele Identifier: CA2699318038

Gene: MSH6 FBXO11

Linked Data

• dbSNP Id: rs2104503408

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804897C>G , CM000664.2:g.47804897C>G	GRCh38
NC_000002.11:g.48032036C>G , CM000664.1:g.48032036C>G	GRCh37
NC_000002.10:g.47885540C>G	NCBI36
NG_007111.1:g.26751C>G , LRG_219:g.26751C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.3142-13C>G (MSH6)	ENSP00000406248.2:n.3142-13C>G
ENST00000420813.6:c.3142-13C>G (MSH6)	ENSP00000390382.2:n.3142-13C>G
ENST00000455383.6:c.3142-13C>G (MSH6)	ENSP00000397484.2:n.3142-13C>G
ENST00000700004.2:c.3173-721C>G (MSH6)	ENSP00000514752.2:n.3173-721C>G
ENST00000699999.1:n.3523-13C>G (MSH6)
ENST00000700000.1:c.1873-13C>G (MSH6)	ENSP00000514749.1:n.1873-13C>G
ENST00000700002.1:c.3445-13C>G (MSH6)	ENSP00000514750.1:n.3445-13C>G
ENST00000700003.1:c.894-13C>G (MSH6)	ENSP00000514751.1:n.894-13C>G
ENST00000700004.1:c.2330-721C>G (MSH6)	ENSP00000514752.1:n.2330-721C>G
ENST00000700005.1:n.2290-13C>G (MSH6)
ENST00000700006.1:n.3498C>G (MSH6)
ENST00000700007.1:n.1444-13C>G (MSH6)
ENST00000700008.1:n.1018-13C>G (MSH6)
ENST00000700009.1:n.1017-13C>G (MSH6)
ENST00000700010.1:n.848-13C>G (MSH6)
ENST00000700011.1:n.2130C>G (MSH6)
ENST00000234420.11:c.3439-13C>G (MSH6) MANE Select	ENSP00000234420.5:n.3439-13C>G
ENST00000540021.6:c.3049-13C>G (MSH6)	ENSP00000446475.1:n.3049-13C>G
ENST00000652107.1:c.3142-13C>G (MSH6)	ENSP00000498629.1:n.3142-13C>G
ENST00000673637.1:c.3142-13C>G (MSH6)	ENSP00000501310.1:n.3142-13C>G
ENST00000234420.9:c.3439-13C>G (MSH6)	ENSP00000234420.4:n.3439-13C>G
ENST00000405808.5:c.169+3298G>C (FBXO11)	ENSP00000385127.1:n.169+3298G>C
ENST00000434234.5:c.*124+3097G>C (FBXO11)	ENSP00000402692.1:n.*124+3097G>C
ENST00000445503.5:c.*2786-13C>G (MSH6)	ENSP00000405294.1:n.*2786-13C>G
ENST00000538136.1:c.2533-13C>G (MSH6)	ENSP00000438580.1:n.2533-13C>G
ENST00000540021.5:c.3049-13C>G (MSH6)	ENSP00000446475.1:n.3049-13C>G
ENST00000614496.4:c.2533-13C>G (MSH6)	ENSP00000477844.1:n.2533-13C>G
ENST00000622629.4:c.335-5C>G (MSH6)	ENSP00000482078.1:n.335-5C>G
NM_000179.2:c.3439-13C>G , LRG_219t1:c.3439-13C>G (MSH6)	NP_000170.1:n.3439-13C>G
NM_001281492.1:c.3049-13C>G (MSH6)	NP_001268421.1:n.3049-13C>G
NM_001281493.1:c.2533-13C>G (MSH6)	NP_001268422.1:n.2533-13C>G
NM_001281494.1:c.2533-13C>G (MSH6)	NP_001268423.1:n.2533-13C>G
XM_005264271.1:c.3142-13C>G (MSH6)	XP_005264328.1:n.3142-13C>G
XM_011532798.1:c.3256-13C>G (MSH6)	XP_011531100.1:n.3256-13C>G
XM_011532799.1:c.3142-13C>G (MSH6)	XP_011531101.1:n.3142-13C>G
XM_011532800.1:c.3142-13C>G (MSH6)	XP_011531102.1:n.3142-13C>G
XM_024452819.1:c.3439-13C>G (MSH6)	XP_024308587.1:n.3439-13C>G
XM_024452820.1:c.3256-13C>G (MSH6)	XP_024308588.1:n.3256-13C>G
XM_024452821.1:c.3142-13C>G (MSH6)	XP_024308589.1:n.3142-13C>G
XM_024452822.1:c.2533-13C>G (MSH6)	XP_024308590.1:n.2533-13C>G
NM_000179.3:c.3439-13C>G (MSH6) MANE Select	NP_000170.1:n.3439-13C>G
NM_001281492.2:c.3049-13C>G (MSH6)	NP_001268421.1:n.3049-13C>G
NM_001281493.2:c.2533-13C>G (MSH6)	NP_001268422.1:n.2533-13C>G
NM_001281494.2:c.2533-13C>G (MSH6)	NP_001268423.1:n.2533-13C>G