Canonical Allele Identifier: CA2658950462

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47804804-GTTGTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47804807_47804811del , CM000664.2:g.47804807_47804811del	GRCh38
NC_000002.11:g.48031946_48031950del , CM000664.1:g.48031946_48031950del	GRCh37
NC_000002.10:g.47885450_47885454del	NCBI36
NG_007111.1:g.26661_26665del , LRG_219:g.26661_26665del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.3142-103_3142-99del (MSH6)	ENSP00000406248.2:n.3142-103_3142-99del
ENST00000420813.6:c.3142-103_3142-99del (MSH6)	ENSP00000390382.2:n.3142-103_3142-99del
ENST00000455383.6:c.3142-103_3142-99del (MSH6)	ENSP00000397484.2:n.3142-103_3142-99del
ENST00000700004.2:c.3173-811_3173-807del (MSH6)	ENSP00000514752.2:n.3173-811_3173-807del
ENST00000699999.1:n.3523-103_3523-99del (MSH6)
ENST00000700000.1:c.1873-103_1873-99del (MSH6)	ENSP00000514749.1:n.1873-103_1873-99del
ENST00000700002.1:c.3445-103_3445-99del (MSH6)	ENSP00000514750.1:n.3445-103_3445-99del
ENST00000700003.1:c.894-103_894-99del (MSH6)	ENSP00000514751.1:n.894-103_894-99del
ENST00000700004.1:c.2330-811_2330-807del (MSH6)	ENSP00000514752.1:n.2330-811_2330-807del
ENST00000700005.1:n.2290-103_2290-99del (MSH6)
ENST00000700006.1:n.3408_3412del (MSH6)
ENST00000700007.1:n.1444-103_1444-99del (MSH6)
ENST00000700008.1:n.1018-103_1018-99del (MSH6)
ENST00000700009.1:n.1017-103_1017-99del (MSH6)
ENST00000700010.1:n.848-103_848-99del (MSH6)
ENST00000700011.1:n.2040_2044del (MSH6)
ENST00000234420.11:c.3439-103_3439-99del (MSH6) MANE Select	ENSP00000234420.5:n.3439-103_3439-99del
ENST00000540021.6:c.3049-103_3049-99del (MSH6)	ENSP00000446475.1:n.3049-103_3049-99del
ENST00000652107.1:c.3142-103_3142-99del (MSH6)	ENSP00000498629.1:n.3142-103_3142-99del
ENST00000673637.1:c.3142-103_3142-99del (MSH6)	ENSP00000501310.1:n.3142-103_3142-99del
ENST00000234420.9:c.3439-103_3439-99del (MSH6)	ENSP00000234420.4:n.3439-103_3439-99del
ENST00000405808.5:c.169+3386_169+3390del (FBXO11)	ENSP00000385127.1:n.169+3386_169+3390del
ENST00000434234.5:c.*124+3185_*124+3189del (FBXO11)	ENSP00000402692.1:n.*124+3185_*124+3189del
ENST00000445503.5:c.*2786-103_*2786-99del (MSH6)	ENSP00000405294.1:n.*2786-103_*2786-99del
ENST00000538136.1:c.2533-103_2533-99del (MSH6)	ENSP00000438580.1:n.2533-103_2533-99del
ENST00000540021.5:c.3049-103_3049-99del (MSH6)	ENSP00000446475.1:n.3049-103_3049-99del
ENST00000614496.4:c.2533-103_2533-99del (MSH6)	ENSP00000477844.1:n.2533-103_2533-99del
ENST00000622629.4:c.335-95_335-91del (MSH6)	ENSP00000482078.1:n.335-95_335-91del
NM_000179.2:c.3439-103_3439-99del , LRG_219t1:c.3439-103_3439-99del (MSH6)	NP_000170.1:n.3439-103_3439-99del
NM_001281492.1:c.3049-103_3049-99del (MSH6)	NP_001268421.1:n.3049-103_3049-99del
NM_001281493.1:c.2533-103_2533-99del (MSH6)	NP_001268422.1:n.2533-103_2533-99del
NM_001281494.1:c.2533-103_2533-99del (MSH6)	NP_001268423.1:n.2533-103_2533-99del
XM_005264271.1:c.3142-103_3142-99del (MSH6)	XP_005264328.1:n.3142-103_3142-99del
XM_011532798.1:c.3256-103_3256-99del (MSH6)	XP_011531100.1:n.3256-103_3256-99del
XM_011532799.1:c.3142-103_3142-99del (MSH6)	XP_011531101.1:n.3142-103_3142-99del
XM_011532800.1:c.3142-103_3142-99del (MSH6)	XP_011531102.1:n.3142-103_3142-99del
XM_024452819.1:c.3439-103_3439-99del (MSH6)	XP_024308587.1:n.3439-103_3439-99del
XM_024452820.1:c.3256-103_3256-99del (MSH6)	XP_024308588.1:n.3256-103_3256-99del
XM_024452821.1:c.3142-103_3142-99del (MSH6)	XP_024308589.1:n.3142-103_3142-99del
XM_024452822.1:c.2533-103_2533-99del (MSH6)	XP_024308590.1:n.2533-103_2533-99del
NM_000179.3:c.3439-103_3439-99del (MSH6) MANE Select	NP_000170.1:n.3439-103_3439-99del
NM_001281492.2:c.3049-103_3049-99del (MSH6)	NP_001268421.1:n.3049-103_3049-99del
NM_001281493.2:c.2533-103_2533-99del (MSH6)	NP_001268422.1:n.2533-103_2533-99del
NM_001281494.2:c.2533-103_2533-99del (MSH6)	NP_001268423.1:n.2533-103_2533-99del