Canonical Allele Identifier: CA2496038072

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783287_47783288delinsTG , CM000664.2:g.47783287_47783288delinsTG	GRCh38
NC_000002.11:g.48010426_48010427delinsTG , CM000664.1:g.48010426_48010427delinsTG	GRCh37
NC_000002.10:g.47863930_47863931delinsTG	NCBI36
NG_007111.1:g.5141_5142delinsTG , LRG_219:g.5141_5142delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700004.2:c.54_55delinsTG	ENSP00000514752.2:p.Ser18=
ENST00000699999.1:n.138_139delinsTG
ENST00000700000.1:c.54_55delinsTG	ENSP00000514749.1:p.Ser18=
ENST00000700001.1:n.126_127delinsTG
ENST00000700002.1:c.54_55delinsTG	ENSP00000514750.1:p.Ser18=
ENST00000700003.1:c.54_55delinsTG	ENSP00000514751.1:p.Ser18=
ENST00000234420.11:c.54_55delinsTG MANE Select	ENSP00000234420.5:p.Ser18=
ENST00000540021.6:c.54_55delinsTG	ENSP00000446475.1:p.Ser18=
ENST00000652107.1:c.-37-7640_-37-7639delinsTG	ENSP00000498629.1:n.-37-7640_-37-7639delinsTG
ENST00000673637.1:c.-38+56_-38+57delinsTG	ENSP00000501310.1:n.-38+56_-38+57delinsTG
ENST00000673922.1:n.143_144delinsTG
ENST00000234420.9:c.54_55delinsTG	ENSP00000234420.4:p.Ser18=
ENST00000445503.5:c.54_55delinsTG	ENSP00000405294.1:p.Ser18=
ENST00000456246.1:c.54_55delinsTG	ENSP00000410570.1:p.Ser18=
ENST00000493177.1:n.118_119delinsTG
ENST00000540021.5:c.54_55delinsTG	ENSP00000446475.1:p.Ser18=
ENST00000606499.1:c.-37-7640_-37-7639delinsTG	ENSP00000475605.1:n.-37-7640_-37-7639delinsTG
ENST00000614496.4:c.-683_-682delinsTG	ENSP00000477844.1:n.-683_-682delinsTG
ENST00000616033.4:c.54_55delinsTG	ENSP00000480261.1:p.Ser18=
ENST00000622629.4:c.-3043_-3042delinsTG	ENSP00000482078.1:n.-3043_-3042delinsTG
NM_000179.2:c.54_55delinsTG , LRG_219t1:c.54_55delinsTG	NP_000170.1:p.Ser18=
NM_001281492.1:c.54_55delinsTG	NP_001268421.1:p.Ser18=
NM_001281493.1:c.-683_-682delinsTG	NP_001268422.1:n.-683_-682delinsTG
XM_011532800.1:c.-38+56_-38+57delinsTG	XP_011531102.1:n.-38+56_-38+57delinsTG
XM_024452819.1:c.54_55delinsTG	XP_024308587.1:p.Ser18=
XM_024452822.1:c.-683_-682delinsTG	XP_024308590.1:n.-683_-682delinsTG
NM_000179.3:c.54_55delinsTG MANE Select	NP_000170.1:p.Ser18=
NM_001281492.2:c.54_55delinsTG	NP_001268421.1:p.Ser18=
NM_001281493.2:c.-683_-682delinsTG	NP_001268422.1:n.-683_-682delinsTG