Canonical Allele Identifier: CA2496048999

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799788_47799792delinsCAAAG , CM000664.2:g.47799788_47799792delinsCAAAG GRCh38
NC_000002.11:g.48026927_48026931delinsCAAAG , CM000664.1:g.48026927_48026931delinsCAAAG GRCh37
NC_000002.10:g.47880431_47880435delinsCAAAG NCBI36
NG_007111.1:g.21642_21646delinsCAAAG , LRG_219:g.21642_21646delinsCAAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.1508_1512delinsCAAAG (MSH6) ENSP00000406248.2:p.Ser503=
ENST00000420813.6:c.1508_1512delinsCAAAG (MSH6) ENSP00000390382.2:p.Ser503=
ENST00000455383.6:c.1508_1512delinsCAAAG (MSH6) ENSP00000397484.2:p.Ser503=
ENST00000700004.2:c.1805_1809delinsCAAAG (MSH6) ENSP00000514752.2:p.Ser602=
ENST00000699999.1:n.1889_1893delinsCAAAG (MSH6)
ENST00000700000.1:c.1606+199_1606+203delinsCAAAG (MSH6) ENSP00000514749.1:n.1606+199_1606+203deli...
ENST00000700002.1:c.1811_1815delinsCAAAG (MSH6) ENSP00000514750.1:p.Ser604=
ENST00000700003.1:c.628-3632_628-3628delinsCAAAG (MSH6) ENSP00000514751.1:n.628-3632_628-3628deli...
ENST00000700004.1:c.962_966delinsCAAAG (MSH6) ENSP00000514752.1:p.Ser321=
ENST00000234420.11:c.1805_1809delinsCAAAG (MSH6) MANE Select ENSP00000234420.5:p.Ser602=
ENST00000540021.6:c.1415_1419delinsCAAAG (MSH6) ENSP00000446475.1:p.Ser472=
ENST00000652107.1:c.1508_1512delinsCAAAG (MSH6) ENSP00000498629.1:p.Ser503=
ENST00000673637.1:c.1508_1512delinsCAAAG (MSH6) ENSP00000501310.1:p.Ser503=
ENST00000234420.9:c.1805_1809delinsCAAAG (MSH6) ENSP00000234420.4:p.Ser602=
ENST00000405808.5:c.169+8403_169+8407delinsCTTTG (FBXO11) ENSP00000385127.1:n.169+8403_169+8407deli...
ENST00000434234.5:c.*124+8202_*124+8206delinsCTTTG (FBXO11) ENSP00000402692.1:n.*124+8202_*124+8206de...
ENST00000445503.5:c.*1152_*1156delinsCAAAG (MSH6) ENSP00000405294.1:n.*1152_*1156delinsCAAA...
ENST00000538136.1:c.899_903delinsCAAAG (MSH6) ENSP00000438580.1:p.Ser300=
ENST00000540021.5:c.1415_1419delinsCAAAG (MSH6) ENSP00000446475.1:p.Ser472=
ENST00000614496.4:c.899_903delinsCAAAG (MSH6) ENSP00000477844.1:p.Ser300=
ENST00000616033.4:c.1802_1806delinsCAAAG (MSH6) ENSP00000480261.1:p.Ser601=
ENST00000622629.4:c.-1292_-1288delinsCAAAG (MSH6) ENSP00000482078.1:n.-1292_-1288delinsCAAA...
NM_000179.2:c.1805_1809delinsCAAAG , LRG_219t1:c.1805_1809delinsCAAAG (MSH6) NP_000170.1:p.Ser602=
NM_001281492.1:c.1415_1419delinsCAAAG (MSH6) NP_001268421.1:p.Ser472=
NM_001281493.1:c.899_903delinsCAAAG (MSH6) NP_001268422.1:p.Ser300=
NM_001281494.1:c.899_903delinsCAAAG (MSH6) NP_001268423.1:p.Ser300=
XM_005264271.1:c.1508_1512delinsCAAAG (MSH6) XP_005264328.1:p.Ser503=
XM_011532798.1:c.1622_1626delinsCAAAG (MSH6) XP_011531100.1:p.Ser541=
XM_011532799.1:c.1508_1512delinsCAAAG (MSH6) XP_011531101.1:p.Ser503=
XM_011532800.1:c.1508_1512delinsCAAAG (MSH6) XP_011531102.1:p.Ser503=
XM_024452819.1:c.1805_1809delinsCAAAG (MSH6) XP_024308587.1:p.Ser602=
XM_024452820.1:c.1622_1626delinsCAAAG (MSH6) XP_024308588.1:p.Ser541=
XM_024452821.1:c.1508_1512delinsCAAAG (MSH6) XP_024308589.1:p.Ser503=
XM_024452822.1:c.899_903delinsCAAAG (MSH6) XP_024308590.1:p.Ser300=
NM_000179.3:c.1805_1809delinsCAAAG (MSH6) MANE Select NP_000170.1:p.Ser602=
NM_001281492.2:c.1415_1419delinsCAAAG (MSH6) NP_001268421.1:p.Ser472=
NM_001281493.2:c.899_903delinsCAAAG (MSH6) NP_001268422.1:p.Ser300=
NM_001281494.2:c.899_903delinsCAAAG (MSH6) NP_001268423.1:p.Ser300=