Canonical Allele Identifier: CA2496048850

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799609_47799613delinsCAAAG , CM000664.2:g.47799609_47799613delinsCAAAG GRCh38
NC_000002.11:g.48026748_48026752delinsCAAAG , CM000664.1:g.48026748_48026752delinsCAAAG GRCh37
NC_000002.10:g.47880252_47880256delinsCAAAG NCBI36
NG_007111.1:g.21463_21467delinsCAAAG , LRG_219:g.21463_21467delinsCAAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.1329_1333delinsCAAAG (MSH6) ENSP00000406248.2:p.Leu443=
ENST00000420813.6:c.1329_1333delinsCAAAG (MSH6) ENSP00000390382.2:p.Leu443=
ENST00000455383.6:c.1329_1333delinsCAAAG (MSH6) ENSP00000397484.2:p.Leu443=
ENST00000700004.2:c.1626_1630delinsCAAAG (MSH6) ENSP00000514752.2:p.Leu542=
ENST00000699999.1:n.1710_1714delinsCAAAG (MSH6)
ENST00000700000.1:c.1606+20_1606+24delinsCAAAG (MSH6) ENSP00000514749.1:n.1606+20_1606+24delins...
ENST00000700002.1:c.1632_1636delinsCAAAG (MSH6) ENSP00000514750.1:p.Leu544=
ENST00000700003.1:c.627+3546_627+3550delinsCAAAG (MSH6) ENSP00000514751.1:n.627+3546_627+3550deli...
ENST00000700004.1:c.783_787delinsCAAAG (MSH6) ENSP00000514752.1:p.Leu261=
ENST00000234420.11:c.1626_1630delinsCAAAG (MSH6) MANE Select ENSP00000234420.5:p.Leu542=
ENST00000540021.6:c.1236_1240delinsCAAAG (MSH6) ENSP00000446475.1:p.Leu412=
ENST00000652107.1:c.1329_1333delinsCAAAG (MSH6) ENSP00000498629.1:p.Leu443=
ENST00000673637.1:c.1329_1333delinsCAAAG (MSH6) ENSP00000501310.1:p.Leu443=
ENST00000234420.9:c.1626_1630delinsCAAAG (MSH6) ENSP00000234420.4:p.Leu542=
ENST00000405808.5:c.169+8582_169+8586delinsCTTTG (FBXO11) ENSP00000385127.1:n.169+8582_169+8586deli...
ENST00000434234.5:c.*124+8381_*124+8385delinsCTTTG (FBXO11) ENSP00000402692.1:n.*124+8381_*124+8385de...
ENST00000445503.5:c.*973_*977delinsCAAAG (MSH6) ENSP00000405294.1:n.*973_*977delinsCAAAG
ENST00000538136.1:c.720_724delinsCAAAG (MSH6) ENSP00000438580.1:p.Leu240=
ENST00000540021.5:c.1236_1240delinsCAAAG (MSH6) ENSP00000446475.1:p.Leu412=
ENST00000614496.4:c.720_724delinsCAAAG (MSH6) ENSP00000477844.1:p.Leu240=
ENST00000616033.4:c.1623_1627delinsCAAAG (MSH6) ENSP00000480261.1:p.Leu541=
ENST00000622629.4:c.-1471_-1467delinsCAAAG (MSH6) ENSP00000482078.1:n.-1471_-1467delinsCAAA...
NM_000179.2:c.1626_1630delinsCAAAG , LRG_219t1:c.1626_1630delinsCAAAG (MSH6) NP_000170.1:p.Leu542=
NM_001281492.1:c.1236_1240delinsCAAAG (MSH6) NP_001268421.1:p.Leu412=
NM_001281493.1:c.720_724delinsCAAAG (MSH6) NP_001268422.1:p.Leu240=
NM_001281494.1:c.720_724delinsCAAAG (MSH6) NP_001268423.1:p.Leu240=
XM_005264271.1:c.1329_1333delinsCAAAG (MSH6) XP_005264328.1:p.Leu443=
XM_011532798.1:c.1443_1447delinsCAAAG (MSH6) XP_011531100.1:p.Leu481=
XM_011532799.1:c.1329_1333delinsCAAAG (MSH6) XP_011531101.1:p.Leu443=
XM_011532800.1:c.1329_1333delinsCAAAG (MSH6) XP_011531102.1:p.Leu443=
XM_024452819.1:c.1626_1630delinsCAAAG (MSH6) XP_024308587.1:p.Leu542=
XM_024452820.1:c.1443_1447delinsCAAAG (MSH6) XP_024308588.1:p.Leu481=
XM_024452821.1:c.1329_1333delinsCAAAG (MSH6) XP_024308589.1:p.Leu443=
XM_024452822.1:c.720_724delinsCAAAG (MSH6) XP_024308590.1:p.Leu240=
NM_000179.3:c.1626_1630delinsCAAAG (MSH6) MANE Select NP_000170.1:p.Leu542=
NM_001281492.2:c.1236_1240delinsCAAAG (MSH6) NP_001268421.1:p.Leu412=
NM_001281493.2:c.720_724delinsCAAAG (MSH6) NP_001268422.1:p.Leu240=
NM_001281494.2:c.720_724delinsCAAAG (MSH6) NP_001268423.1:p.Leu240=