Canonical Allele Identifier: CA2496048833

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799594_47799598delinsGTATC , CM000664.2:g.47799594_47799598delinsGTATC GRCh38
NC_000002.11:g.48026733_48026737delinsGTATC , CM000664.1:g.48026733_48026737delinsGTATC GRCh37
NC_000002.10:g.47880237_47880241delinsGTATC NCBI36
NG_007111.1:g.21448_21452delinsGTATC , LRG_219:g.21448_21452delinsGTATC

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.1314_1318delinsGTATC (MSH6) ENSP00000406248.2:p.Lys438=
ENST00000420813.6:c.1314_1318delinsGTATC (MSH6) ENSP00000390382.2:p.Lys438=
ENST00000455383.6:c.1314_1318delinsGTATC (MSH6) ENSP00000397484.2:p.Lys438=
ENST00000700004.2:c.1611_1615delinsGTATC (MSH6) ENSP00000514752.2:p.Lys537=
ENST00000699999.1:n.1695_1699delinsGTATC (MSH6)
ENST00000700000.1:c.1606+5_1606+9delinsGTATC (MSH6) ENSP00000514749.1:n.1606+5_1606+9delinsGT...
ENST00000700002.1:c.1617_1621delinsGTATC (MSH6) ENSP00000514750.1:p.Lys539=
ENST00000700003.1:c.627+3531_627+3535delinsGTATC (MSH6) ENSP00000514751.1:n.627+3531_627+3535deli...
ENST00000700004.1:c.768_772delinsGTATC (MSH6) ENSP00000514752.1:p.Lys256=
ENST00000234420.11:c.1611_1615delinsGTATC (MSH6) MANE Select ENSP00000234420.5:p.Lys537=
ENST00000540021.6:c.1221_1225delinsGTATC (MSH6) ENSP00000446475.1:p.Lys407=
ENST00000652107.1:c.1314_1318delinsGTATC (MSH6) ENSP00000498629.1:p.Lys438=
ENST00000673637.1:c.1314_1318delinsGTATC (MSH6) ENSP00000501310.1:p.Lys438=
ENST00000234420.9:c.1611_1615delinsGTATC (MSH6) ENSP00000234420.4:p.Lys537=
ENST00000405808.5:c.169+8597_169+8601delinsGATAC (FBXO11) ENSP00000385127.1:n.169+8597_169+8601deli...
ENST00000434234.5:c.*124+8396_*124+8400delinsGATAC (FBXO11) ENSP00000402692.1:n.*124+8396_*124+8400de...
ENST00000445503.5:c.*958_*962delinsGTATC (MSH6) ENSP00000405294.1:n.*958_*962delinsGTATC
ENST00000538136.1:c.705_709delinsGTATC (MSH6) ENSP00000438580.1:p.Lys235=
ENST00000540021.5:c.1221_1225delinsGTATC (MSH6) ENSP00000446475.1:p.Lys407=
ENST00000614496.4:c.705_709delinsGTATC (MSH6) ENSP00000477844.1:p.Lys235=
ENST00000616033.4:c.1608_1612delinsGTATC (MSH6) ENSP00000480261.1:p.Lys536=
ENST00000622629.4:c.-1486_-1482delinsGTATC (MSH6) ENSP00000482078.1:n.-1486_-1482delinsGTAT...
NM_000179.2:c.1611_1615delinsGTATC , LRG_219t1:c.1611_1615delinsGTATC (MSH6) NP_000170.1:p.Lys537=
NM_001281492.1:c.1221_1225delinsGTATC (MSH6) NP_001268421.1:p.Lys407=
NM_001281493.1:c.705_709delinsGTATC (MSH6) NP_001268422.1:p.Lys235=
NM_001281494.1:c.705_709delinsGTATC (MSH6) NP_001268423.1:p.Lys235=
XM_005264271.1:c.1314_1318delinsGTATC (MSH6) XP_005264328.1:p.Lys438=
XM_011532798.1:c.1428_1432delinsGTATC (MSH6) XP_011531100.1:p.Lys476=
XM_011532799.1:c.1314_1318delinsGTATC (MSH6) XP_011531101.1:p.Lys438=
XM_011532800.1:c.1314_1318delinsGTATC (MSH6) XP_011531102.1:p.Lys438=
XM_024452819.1:c.1611_1615delinsGTATC (MSH6) XP_024308587.1:p.Lys537=
XM_024452820.1:c.1428_1432delinsGTATC (MSH6) XP_024308588.1:p.Lys476=
XM_024452821.1:c.1314_1318delinsGTATC (MSH6) XP_024308589.1:p.Lys438=
XM_024452822.1:c.705_709delinsGTATC (MSH6) XP_024308590.1:p.Lys235=
NM_000179.3:c.1611_1615delinsGTATC (MSH6) MANE Select NP_000170.1:p.Lys537=
NM_001281492.2:c.1221_1225delinsGTATC (MSH6) NP_001268421.1:p.Lys407=
NM_001281493.2:c.705_709delinsGTATC (MSH6) NP_001268422.1:p.Lys235=
NM_001281494.2:c.705_709delinsGTATC (MSH6) NP_001268423.1:p.Lys235=