Canonical Allele Identifier: CA658655622
Gene: MSH6 HGNC NCBI

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
ENST00000234420.11:c.460_3646+2del
ENST00000540021.6:c.238-2715_3256+2del
ENST00000652107.1:c.163_3349+2del
ENST00000673637.1:c.163_3349+2del
ENST00000234420.9:c.460_3646+2del
ENST00000405808.5:c.169+2491_170-6451del ENSP00000385127.1:p.=
ENST00000434234.5:c.*124+2290_*125-6451del ENSP00000402692.1:p.=
ENST00000445503.5:c.458-2715_*2993+2del
ENST00000538136.1:c.-443_2740+2del
ENST00000540021.5:c.238-2715_3256+2del
ENST00000614496.4:c.-279-2715_2740+2del
ENST00000622629.4:c.-2637_550+2del
NM_000179.2:c.460_3646+2del , LRG_219t1:c.460_3646+2del
NM_001281492.1:c.238-2715_3256+2del
NM_001281493.1:c.-279-2715_2740+2del
NM_001281494.1:c.-443_2740+2del
XM_005264271.1:c.163_3349+2del
XM_011532798.1:c.277_3463+2del
XM_011532799.1:c.163_3349+2del
XM_011532800.1:c.163_3349+2del
XM_024452819.1:c.460_3646+2del
XM_024452820.1:c.277_3463+2del
XM_024452821.1:c.163_3349+2del
XM_024452822.1:c.-279-2715_2740+2del
NM_000179.3:c.460_3646+2del
NM_001281492.2:c.238-2715_3256+2del
NM_001281493.2:c.-279-2715_2740+2del
NM_001281494.2:c.-443_2740+2del