Canonical Allele Identifier: CA2658950216

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47803342-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803345del , CM000664.2:g.47803345del	GRCh38
NC_000002.11:g.48030484del , CM000664.1:g.48030484del	GRCh37
NC_000002.10:g.47883988del	NCBI36
NG_007111.1:g.25199del , LRG_219:g.25199del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.2876-75del (MSH6)	ENSP00000406248.2:n.2876-75del
ENST00000420813.6:c.2876-75del (MSH6)	ENSP00000390382.2:n.2876-75del
ENST00000455383.6:c.2876-75del (MSH6)	ENSP00000397484.2:n.2876-75del
ENST00000700004.2:c.3172+2190del (MSH6)	ENSP00000514752.2:n.3172+2190del
ENST00000699999.1:n.3257-75del (MSH6)
ENST00000700000.1:c.1607-75del (MSH6)	ENSP00000514749.1:n.1607-75del
ENST00000700002.1:c.3179-75del (MSH6)	ENSP00000514750.1:n.3179-75del
ENST00000700003.1:c.628-75del (MSH6)	ENSP00000514751.1:n.628-75del
ENST00000700004.1:c.2329+2190del (MSH6)	ENSP00000514752.1:n.2329+2190del
ENST00000700005.1:n.1949del (MSH6)
ENST00000700006.1:n.1946del (MSH6)
ENST00000700007.1:n.1103del (MSH6)
ENST00000700008.1:n.677del (MSH6)
ENST00000700009.1:n.676del (MSH6)
ENST00000700010.1:n.582-75del (MSH6)
ENST00000700011.1:n.578del (MSH6)
ENST00000234420.11:c.3173-75del (MSH6) MANE Select	ENSP00000234420.5:n.3173-75del
ENST00000540021.6:c.2783-75del (MSH6)	ENSP00000446475.1:n.2783-75del
ENST00000652107.1:c.2876-75del (MSH6)	ENSP00000498629.1:n.2876-75del
ENST00000673637.1:c.2876-75del (MSH6)	ENSP00000501310.1:n.2876-75del
ENST00000234420.9:c.3173-75del (MSH6)	ENSP00000234420.4:n.3173-75del
ENST00000405808.5:c.169+4852del (FBXO11)	ENSP00000385127.1:n.169+4852del
ENST00000434234.5:c.*124+4651del (FBXO11)	ENSP00000402692.1:n.*124+4651del
ENST00000445503.5:c.*2520-75del (MSH6)	ENSP00000405294.1:n.*2520-75del
ENST00000538136.1:c.2267-75del (MSH6)	ENSP00000438580.1:n.2267-75del
ENST00000540021.5:c.2783-75del (MSH6)	ENSP00000446475.1:n.2783-75del
ENST00000614496.4:c.2267-75del (MSH6)	ENSP00000477844.1:n.2267-75del
ENST00000622629.4:c.77-75del (MSH6)	ENSP00000482078.1:n.77-75del
NM_000179.2:c.3173-75del , LRG_219t1:c.3173-75del (MSH6)	NP_000170.1:n.3173-75del
NM_001281492.1:c.2783-75del (MSH6)	NP_001268421.1:n.2783-75del
NM_001281493.1:c.2267-75del (MSH6)	NP_001268422.1:n.2267-75del
NM_001281494.1:c.2267-75del (MSH6)	NP_001268423.1:n.2267-75del
XM_005264271.1:c.2876-75del (MSH6)	XP_005264328.1:n.2876-75del
XM_011532798.1:c.2990-75del (MSH6)	XP_011531100.1:n.2990-75del
XM_011532799.1:c.2876-75del (MSH6)	XP_011531101.1:n.2876-75del
XM_011532800.1:c.2876-75del (MSH6)	XP_011531102.1:n.2876-75del
XM_024452819.1:c.3173-75del (MSH6)	XP_024308587.1:n.3173-75del
XM_024452820.1:c.2990-75del (MSH6)	XP_024308588.1:n.2990-75del
XM_024452821.1:c.2876-75del (MSH6)	XP_024308589.1:n.2876-75del
XM_024452822.1:c.2267-75del (MSH6)	XP_024308590.1:n.2267-75del
NM_000179.3:c.3173-75del (MSH6) MANE Select	NP_000170.1:n.3173-75del
NM_001281492.2:c.2783-75del (MSH6)	NP_001268421.1:n.2783-75del
NM_001281493.2:c.2267-75del (MSH6)	NP_001268422.1:n.2267-75del
NM_001281494.2:c.2267-75del (MSH6)	NP_001268423.1:n.2267-75del