Canonical Allele Identifier: CA2739274372

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 2824794
• ClinVar RCV Id: RCV003761067

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804903_47804906del , CM000664.2:g.47804903_47804906del	GRCh38
NC_000002.11:g.48032042_48032045del , CM000664.1:g.48032042_48032045del	GRCh37
NC_000002.10:g.47885546_47885549del	NCBI36
NG_007111.1:g.26757_26760del , LRG_219:g.26757_26760del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3142-7_3142-4del (MSH6)	ENSP00000406248.2:n.3142-7_3142-4del
ENST00000420813.6:c.3142-7_3142-4del (MSH6)	ENSP00000390382.2:n.3142-7_3142-4del
ENST00000455383.6:c.3142-7_3142-4del (MSH6)	ENSP00000397484.2:n.3142-7_3142-4del
ENST00000700004.2:c.3173-715_3173-712del (MSH6)	ENSP00000514752.2:n.3173-715_3173-712del
ENST00000699999.1:n.3523-7_3523-4del (MSH6)
ENST00000700000.1:c.1873-7_1873-4del (MSH6)	ENSP00000514749.1:n.1873-7_1873-4del
ENST00000700002.1:c.3445-7_3445-4del (MSH6)	ENSP00000514750.1:n.3445-7_3445-4del
ENST00000700003.1:c.894-7_894-4del (MSH6)	ENSP00000514751.1:n.894-7_894-4del
ENST00000700004.1:c.2330-715_2330-712del (MSH6)	ENSP00000514752.1:n.2330-715_2330-712del
ENST00000700005.1:n.2290-7_2290-4del (MSH6)
ENST00000700006.1:n.3504_3507del (MSH6)
ENST00000700007.1:n.1444-7_1444-4del (MSH6)
ENST00000700008.1:n.1018-7_1018-4del (MSH6)
ENST00000700009.1:n.1017-7_1017-4del (MSH6)
ENST00000700010.1:n.848-7_848-4del (MSH6)
ENST00000700011.1:n.2136_2139del (MSH6)
ENST00000234420.11:c.3439-7_3439-4del (MSH6) MANE Select	ENSP00000234420.5:n.3439-7_3439-4del
ENST00000540021.6:c.3049-7_3049-4del (MSH6)	ENSP00000446475.1:n.3049-7_3049-4del
ENST00000652107.1:c.3142-7_3142-4del (MSH6)	ENSP00000498629.1:n.3142-7_3142-4del
ENST00000673637.1:c.3142-7_3142-4del (MSH6)	ENSP00000501310.1:n.3142-7_3142-4del
ENST00000234420.9:c.3439-7_3439-4del (MSH6)	ENSP00000234420.4:n.3439-7_3439-4del
ENST00000405808.5:c.169+3292_169+3295del (FBXO11)	ENSP00000385127.1:n.169+3292_169+3295del
ENST00000434234.5:c.*124+3091_*124+3094del (FBXO11)	ENSP00000402692.1:n.*124+3091_*124+3094del
ENST00000445503.5:c.*2786-7_*2786-4del (MSH6)	ENSP00000405294.1:n.*2786-7_*2786-4del
ENST00000538136.1:c.2533-7_2533-4del (MSH6)	ENSP00000438580.1:n.2533-7_2533-4del
ENST00000540021.5:c.3049-7_3049-4del (MSH6)	ENSP00000446475.1:n.3049-7_3049-4del
ENST00000614496.4:c.2533-7_2533-4del (MSH6)	ENSP00000477844.1:n.2533-7_2533-4del
ENST00000622629.4:c.336_339del (MSH6)
NM_000179.2:c.3439-7_3439-4del , LRG_219t1:c.3439-7_3439-4del (MSH6)	NP_000170.1:n.3439-7_3439-4del
NM_001281492.1:c.3049-7_3049-4del (MSH6)	NP_001268421.1:n.3049-7_3049-4del
NM_001281493.1:c.2533-7_2533-4del (MSH6)	NP_001268422.1:n.2533-7_2533-4del
NM_001281494.1:c.2533-7_2533-4del (MSH6)	NP_001268423.1:n.2533-7_2533-4del
XM_005264271.1:c.3142-7_3142-4del (MSH6)	XP_005264328.1:n.3142-7_3142-4del
XM_011532798.1:c.3256-7_3256-4del (MSH6)	XP_011531100.1:n.3256-7_3256-4del
XM_011532799.1:c.3142-7_3142-4del (MSH6)	XP_011531101.1:n.3142-7_3142-4del
XM_011532800.1:c.3142-7_3142-4del (MSH6)	XP_011531102.1:n.3142-7_3142-4del
XM_024452819.1:c.3439-7_3439-4del (MSH6)	XP_024308587.1:n.3439-7_3439-4del
XM_024452820.1:c.3256-7_3256-4del (MSH6)	XP_024308588.1:n.3256-7_3256-4del
XM_024452821.1:c.3142-7_3142-4del (MSH6)	XP_024308589.1:n.3142-7_3142-4del
XM_024452822.1:c.2533-7_2533-4del (MSH6)	XP_024308590.1:n.2533-7_2533-4del
NM_000179.3:c.3439-7_3439-4del (MSH6) MANE Select	NP_000170.1:n.3439-7_3439-4del
NM_001281492.2:c.3049-7_3049-4del (MSH6)	NP_001268421.1:n.3049-7_3049-4del
NM_001281493.2:c.2533-7_2533-4del (MSH6)	NP_001268422.1:n.2533-7_2533-4del
NM_001281494.2:c.2533-7_2533-4del (MSH6)	NP_001268423.1:n.2533-7_2533-4del