Canonical Allele Identifier: CA2496038029

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783239_47783240delinsGC , CM000664.2:g.47783239_47783240delinsGC	GRCh38
NC_000002.11:g.48010378_48010379delinsGC , CM000664.1:g.48010378_48010379delinsGC	GRCh37
NC_000002.10:g.47863882_47863883delinsGC	NCBI36
NG_007111.1:g.5093_5094delinsGC , LRG_219:g.5093_5094delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700004.2:c.6_7delinsGC	ENSP00000514752.2:p.Ser2=
ENST00000699999.1:n.90_91delinsGC
ENST00000700000.1:c.6_7delinsGC	ENSP00000514749.1:p.Ser2=
ENST00000700001.1:n.78_79delinsGC
ENST00000700002.1:c.6_7delinsGC	ENSP00000514750.1:p.Ser2=
ENST00000700003.1:c.6_7delinsGC	ENSP00000514751.1:p.Ser2=
ENST00000234420.11:c.6_7delinsGC MANE Select	ENSP00000234420.5:p.Ser2=
ENST00000540021.6:c.6_7delinsGC	ENSP00000446475.1:p.Ser2=
ENST00000652107.1:c.-37-7688_-37-7687delinsGC	ENSP00000498629.1:n.-37-7688_-37-7687delinsGC
ENST00000673637.1:c.-38+8_-38+9delinsGC	ENSP00000501310.1:n.-38+8_-38+9delinsGC
ENST00000673922.1:n.95_96delinsGC
ENST00000234420.9:c.6_7delinsGC	ENSP00000234420.4:p.Ser2=
ENST00000445503.5:c.6_7delinsGC	ENSP00000405294.1:p.Ser2=
ENST00000456246.1:c.6_7delinsGC	ENSP00000410570.1:p.Ser2=
ENST00000493177.1:n.70_71delinsGC
ENST00000540021.5:c.6_7delinsGC	ENSP00000446475.1:p.Ser2=
ENST00000606499.1:c.-37-7688_-37-7687delinsGC	ENSP00000475605.1:n.-37-7688_-37-7687delinsGC
ENST00000614496.4:c.-731_-730delinsGC	ENSP00000477844.1:n.-731_-730delinsGC
ENST00000616033.4:c.6_7delinsGC	ENSP00000480261.1:p.Ser2=
ENST00000622629.4:c.-3091_-3090delinsGC	ENSP00000482078.1:n.-3091_-3090delinsGC
NM_000179.2:c.6_7delinsGC , LRG_219t1:c.6_7delinsGC	NP_000170.1:p.Ser2=
NM_001281492.1:c.6_7delinsGC	NP_001268421.1:p.Ser2=
NM_001281493.1:c.-731_-730delinsGC	NP_001268422.1:n.-731_-730delinsGC
XM_011532800.1:c.-38+8_-38+9delinsGC	XP_011531102.1:n.-38+8_-38+9delinsGC
XM_024452819.1:c.6_7delinsGC	XP_024308587.1:p.Ser2=
XM_024452822.1:c.-731_-730delinsGC	XP_024308590.1:n.-731_-730delinsGC
NM_000179.3:c.6_7delinsGC MANE Select	NP_000170.1:p.Ser2=
NM_001281492.2:c.6_7delinsGC	NP_001268421.1:p.Ser2=
NM_001281493.2:c.-731_-730delinsGC	NP_001268422.1:n.-731_-730delinsGC