Canonical Allele Identifier: CA658655622

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47795896_47805709del , CM000664.2:g.47795896_47805709del GRCh38
NC_000002.11:g.48023035_48032848del , CM000664.1:g.48023035_48032848del GRCh37
NC_000002.10:g.47876539_47886352del NCBI36
NG_007111.1:g.17750_27563del , LRG_219:g.17750_27563del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.163_3349+2del (MSH6)
ENST00000420813.6:c.163_3349+2del (MSH6)
ENST00000455383.6:c.163_3349+2del (MSH6)
ENST00000700004.2:c.460_3262+2del (MSH6)
ENST00000699999.1:n.544_4320+2del (MSH6)
ENST00000700000.1:c.460_2080+2del (MSH6)
ENST00000700002.1:c.460_3652+2del (MSH6)
ENST00000700003.1:c.460_1101+2del (MSH6)
ENST00000234420.11:c.460_3646+2del (MSH6)
ENST00000540021.6:c.238-2715_3256+2del (MSH6)
ENST00000652107.1:c.163_3349+2del (MSH6)
ENST00000673637.1:c.163_3349+2del (MSH6)
ENST00000234420.9:c.460_3646+2del (MSH6)
ENST00000405808.5:c.169+2491_170-6451del (FBXO11) ENSP00000385127.1:n.169+2491_170-6451del
ENST00000434234.5:c.*124+2290_*125-6451del (FBXO11) ENSP00000402692.1:n.*124+2290_*125-6451de...
ENST00000445503.5:c.458-2715_*2993+2del (MSH6)
ENST00000538136.1:c.-443_2740+2del (MSH6)
ENST00000540021.5:c.238-2715_3256+2del (MSH6)
ENST00000614496.4:c.-279-2715_2740+2del (MSH6)
ENST00000622629.4:c.-2637_550+2del (MSH6)
NM_000179.2:c.460_3646+2del , LRG_219t1:c.460_3646+2del (MSH6)
NM_001281492.1:c.238-2715_3256+2del (MSH6)
NM_001281493.1:c.-279-2715_2740+2del (MSH6)
NM_001281494.1:c.-443_2740+2del (MSH6)
XM_005264271.1:c.163_3349+2del (MSH6)
XM_011532798.1:c.277_3463+2del (MSH6)
XM_011532799.1:c.163_3349+2del (MSH6)
XM_011532800.1:c.163_3349+2del (MSH6)
XM_024452819.1:c.460_3646+2del (MSH6)
XM_024452820.1:c.277_3463+2del (MSH6)
XM_024452821.1:c.163_3349+2del (MSH6)
XM_024452822.1:c.-279-2715_2740+2del (MSH6)
NM_000179.3:c.460_3646+2del (MSH6)
NM_001281492.2:c.238-2715_3256+2del (MSH6)
NM_001281493.2:c.-279-2715_2740+2del (MSH6)
NM_001281494.2:c.-443_2740+2del (MSH6)