Canonical Allele Identifier: CA2658966538

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47805584-ATGAGTATTCATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47805587_47805598del , CM000664.2:g.47805587_47805598del	GRCh38
NC_000002.11:g.48032726_48032737del , CM000664.1:g.48032726_48032737del	GRCh37
NC_000002.10:g.47886230_47886241del	NCBI36
NG_007111.1:g.27441_27452del , LRG_219:g.27441_27452del
NG_008397.1:g.105080_105091del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3260-31_3260-20del (MSH6)	ENSP00000406248.2:n.3260-31_3260-20del
ENST00000420813.6:c.3260-31_3260-20del (MSH6)	ENSP00000390382.2:n.3260-31_3260-20del
ENST00000455383.6:c.3260-31_3260-20del (MSH6)	ENSP00000397484.2:n.3260-31_3260-20del
ENST00000700004.2:c.3173-31_3173-20del (MSH6)	ENSP00000514752.2:n.3173-31_3173-20del
ENST00000699999.1:n.4200_4211del (MSH6)
ENST00000700000.1:c.1991-31_1991-20del (MSH6)	ENSP00000514749.1:n.1991-31_1991-20del
ENST00000700002.1:c.3563-31_3563-20del (MSH6)	ENSP00000514750.1:n.3563-31_3563-20del
ENST00000700003.1:c.1012-31_1012-20del (MSH6)	ENSP00000514751.1:n.1012-31_1012-20del
ENST00000700004.1:c.2330-31_2330-20del (MSH6)	ENSP00000514752.1:n.2330-31_2330-20del
ENST00000700005.1:n.2408-31_2408-20del (MSH6)
ENST00000700006.1:n.4188_4199del (MSH6)
ENST00000700007.1:n.2121_2132del (MSH6)
ENST00000700008.1:n.1695_1706del (MSH6)
ENST00000700009.1:n.1694_1705del (MSH6)
ENST00000700010.1:n.966-31_966-20del (MSH6)
ENST00000700011.1:n.2820_2831del (MSH6)
ENST00000234420.11:c.3557-31_3557-20del (MSH6) MANE Select	ENSP00000234420.5:n.3557-31_3557-20del
ENST00000540021.6:c.3167-31_3167-20del (MSH6)	ENSP00000446475.1:n.3167-31_3167-20del
ENST00000652107.1:c.3260-31_3260-20del (MSH6)	ENSP00000498629.1:n.3260-31_3260-20del
ENST00000673637.1:c.3260-31_3260-20del (MSH6)	ENSP00000501310.1:n.3260-31_3260-20del
ENST00000234420.9:c.3557-31_3557-20del (MSH6)	ENSP00000234420.4:n.3557-31_3557-20del
ENST00000405808.5:c.169+2599_169+2610del (FBXO11)	ENSP00000385127.1:n.169+2599_169+2610del
ENST00000434234.5:c.*124+2398_*124+2409del (FBXO11)	ENSP00000402692.1:n.*124+2398_*124+2409del
ENST00000445503.5:c.*2904-31_*2904-20del (MSH6)	ENSP00000405294.1:n.*2904-31_*2904-20del
ENST00000538136.1:c.2651-31_2651-20del (MSH6)	ENSP00000438580.1:n.2651-31_2651-20del
ENST00000540021.5:c.3167-31_3167-20del (MSH6)	ENSP00000446475.1:n.3167-31_3167-20del
ENST00000614496.4:c.2651-31_2651-20del (MSH6)	ENSP00000477844.1:n.2651-31_2651-20del
ENST00000622629.4:c.461-31_461-20del (MSH6)	ENSP00000482078.1:n.461-31_461-20del
NM_000179.2:c.3557-31_3557-20del , LRG_219t1:c.3557-31_3557-20del (MSH6)	NP_000170.1:n.3557-31_3557-20del
NM_001281492.1:c.3167-31_3167-20del (MSH6)	NP_001268421.1:n.3167-31_3167-20del
NM_001281493.1:c.2651-31_2651-20del (MSH6)	NP_001268422.1:n.2651-31_2651-20del
NM_001281494.1:c.2651-31_2651-20del (MSH6)	NP_001268423.1:n.2651-31_2651-20del
XM_005264271.1:c.3260-31_3260-20del (MSH6)	XP_005264328.1:n.3260-31_3260-20del
XM_011532798.1:c.3374-31_3374-20del (MSH6)	XP_011531100.1:n.3374-31_3374-20del
XM_011532799.1:c.3260-31_3260-20del (MSH6)	XP_011531101.1:n.3260-31_3260-20del
XM_011532800.1:c.3260-31_3260-20del (MSH6)	XP_011531102.1:n.3260-31_3260-20del
XM_024452819.1:c.3557-31_3557-20del (MSH6)	XP_024308587.1:n.3557-31_3557-20del
XM_024452820.1:c.3374-31_3374-20del (MSH6)	XP_024308588.1:n.3374-31_3374-20del
XM_024452821.1:c.3260-31_3260-20del (MSH6)	XP_024308589.1:n.3260-31_3260-20del
XM_024452822.1:c.2651-31_2651-20del (MSH6)	XP_024308590.1:n.2651-31_2651-20del
NM_000179.3:c.3557-31_3557-20del (MSH6) MANE Select	NP_000170.1:n.3557-31_3557-20del
NM_001281492.2:c.3167-31_3167-20del (MSH6)	NP_001268421.1:n.3167-31_3167-20del
NM_001281493.2:c.2651-31_2651-20del (MSH6)	NP_001268422.1:n.2651-31_2651-20del
NM_001281494.2:c.2651-31_2651-20del (MSH6)	NP_001268423.1:n.2651-31_2651-20del