Canonical Allele Identifier: CA2496038083
Gene: MSH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783296_47783299delinsCAAG , CM000664.2:g.47783296_47783299delinsCAAG GRCh38
NC_000002.11:g.48010435_48010438delinsCAAG , CM000664.1:g.48010435_48010438delinsCAAG GRCh37
NC_000002.10:g.47863939_47863942delinsCAAG NCBI36
NG_007111.1:g.5150_5153delinsCAAG , LRG_219:g.5150_5153delinsCAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700004.2:c.63_66delinsCAAG ENSP00000514752.2:p.Asn21=
ENST00000699999.1:n.147_150delinsCAAG
ENST00000700000.1:c.63_66delinsCAAG ENSP00000514749.1:p.Asn21=
ENST00000700001.1:n.135_138delinsCAAG
ENST00000700002.1:c.63_66delinsCAAG ENSP00000514750.1:p.Asn21=
ENST00000700003.1:c.63_66delinsCAAG ENSP00000514751.1:p.Asn21=
ENST00000234420.11:c.63_66delinsCAAG MANE Select ENSP00000234420.5:p.Asn21=
ENST00000540021.6:c.63_66delinsCAAG ENSP00000446475.1:p.Asn21=
ENST00000652107.1:c.-37-7631_-37-7628delinsCAAG ENSP00000498629.1:n.-37-7631_-37-7628delinsCAAG
ENST00000673637.1:c.-38+65_-38+68delinsCAAG ENSP00000501310.1:n.-38+65_-38+68delinsCAAG
ENST00000673922.1:n.152_155delinsCAAG
ENST00000234420.9:c.63_66delinsCAAG ENSP00000234420.4:p.Asn21=
ENST00000445503.5:c.63_66delinsCAAG ENSP00000405294.1:p.Asn21=
ENST00000456246.1:c.63_66delinsCAAG ENSP00000410570.1:p.Asn21=
ENST00000493177.1:n.127_130delinsCAAG
ENST00000540021.5:c.63_66delinsCAAG ENSP00000446475.1:p.Asn21=
ENST00000606499.1:c.-37-7631_-37-7628delinsCAAG ENSP00000475605.1:n.-37-7631_-37-7628delinsCAAG
ENST00000614496.4:c.-674_-671delinsCAAG ENSP00000477844.1:n.-674_-671delinsCAAG
ENST00000616033.4:c.63_66delinsCAAG ENSP00000480261.1:p.Asn21=
ENST00000622629.4:c.-3034_-3031delinsCAAG ENSP00000482078.1:n.-3034_-3031delinsCAAG
NM_000179.2:c.63_66delinsCAAG , LRG_219t1:c.63_66delinsCAAG NP_000170.1:p.Asn21=
NM_001281492.1:c.63_66delinsCAAG NP_001268421.1:p.Asn21=
NM_001281493.1:c.-674_-671delinsCAAG NP_001268422.1:n.-674_-671delinsCAAG
XM_011532800.1:c.-38+65_-38+68delinsCAAG XP_011531102.1:n.-38+65_-38+68delinsCAAG
XM_024452819.1:c.63_66delinsCAAG XP_024308587.1:p.Asn21=
XM_024452822.1:c.-674_-671delinsCAAG XP_024308590.1:n.-674_-671delinsCAAG
NM_000179.3:c.63_66delinsCAAG MANE Select NP_000170.1:p.Asn21=
NM_001281492.2:c.63_66delinsCAAG NP_001268421.1:p.Asn21=
NM_001281493.2:c.-674_-671delinsCAAG NP_001268422.1:n.-674_-671delinsCAAG