Canonical Allele Identifier: CA2496038473

Gene: MSH6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783725_47783726delinsAG , CM000664.2:g.47783725_47783726delinsAG	GRCh38
NC_000002.11:g.48010864_48010865delinsAG , CM000664.1:g.48010864_48010865delinsAG	GRCh37
NC_000002.10:g.47864368_47864369delinsAG	NCBI36
NG_007111.1:g.5579_5580delinsAG , LRG_219:g.5579_5580delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455383.6:c.-91_-90delinsAG	ENSP00000397484.2:n.-91_-90delinsAG
ENST00000700004.2:c.260+232_260+233delinsAG	ENSP00000514752.2:n.260+232_260+233delinsAG
ENST00000699999.1:n.344+232_344+233delinsAG
ENST00000700000.1:c.260+232_260+233delinsAG	ENSP00000514749.1:n.260+232_260+233delinsAG
ENST00000700001.1:n.332+232_332+233delinsAG
ENST00000700002.1:c.260+232_260+233delinsAG	ENSP00000514750.1:n.260+232_260+233delinsAG
ENST00000700003.1:c.260+232_260+233delinsAG	ENSP00000514751.1:n.260+232_260+233delinsAG
ENST00000234420.11:c.260+232_260+233delinsAG MANE Select	ENSP00000234420.5:n.260+232_260+233delinsAG
ENST00000540021.6:c.237+255_237+256delinsAG	ENSP00000446475.1:n.237+255_237+256delinsAG
ENST00000652107.1:c.-37-7202_-37-7201delinsAG	ENSP00000498629.1:n.-37-7202_-37-7201delinsAG
ENST00000673637.1:c.-38+494_-38+495delinsAG	ENSP00000501310.1:n.-38+494_-38+495delinsAG
ENST00000673922.1:n.349+232_349+233delinsAG
ENST00000234420.9:c.260+232_260+233delinsAG	ENSP00000234420.4:n.260+232_260+233delinsAG
ENST00000445503.5:c.260+232_260+233delinsAG	ENSP00000405294.1:n.260+232_260+233delinsAG
ENST00000455383.5:c.-91_-90delinsAG	ENSP00000397484.1:n.-91_-90delinsAG
ENST00000456246.1:c.260+232_260+233delinsAG	ENSP00000410570.1:n.260+232_260+233delinsAG
ENST00000493177.1:n.324+232_324+233delinsAG
ENST00000540021.5:c.237+255_237+256delinsAG	ENSP00000446475.1:n.237+255_237+256delinsAG
ENST00000606499.1:c.-37-7202_-37-7201delinsAG	ENSP00000475605.1:n.-37-7202_-37-7201delinsAG
ENST00000614496.4:c.-477+232_-477+233delinsAG	ENSP00000477844.1:n.-477+232_-477+233delinsAG
ENST00000616033.4:c.257+232_257+233delinsAG	ENSP00000480261.1:n.257+232_257+233delinsAG
ENST00000622629.4:c.-2837+232_-2837+233delinsAG	ENSP00000482078.1:n.-2837+232_-2837+233delinsAG
NM_000179.2:c.260+232_260+233delinsAG , LRG_219t1:c.260+232_260+233delinsAG	NP_000170.1:n.260+232_260+233delinsAG
NM_001281492.1:c.237+255_237+256delinsAG	NP_001268421.1:n.237+255_237+256delinsAG
NM_001281493.1:c.-477+232_-477+233delinsAG	NP_001268422.1:n.-477+232_-477+233delinsAG
XM_011532799.1:c.-91_-90delinsAG	XP_011531101.1:n.-91_-90delinsAG
XM_011532800.1:c.-38+494_-38+495delinsAG	XP_011531102.1:n.-38+494_-38+495delinsAG
XM_024452819.1:c.260+232_260+233delinsAG	XP_024308587.1:n.260+232_260+233delinsAG
XM_024452821.1:c.-91_-90delinsAG	XP_024308589.1:n.-91_-90delinsAG
XM_024452822.1:c.-477+232_-477+233delinsAG	XP_024308590.1:n.-477+232_-477+233delinsAG
NM_000179.3:c.260+232_260+233delinsAG MANE Select	NP_000170.1:n.260+232_260+233delinsAG
NM_001281492.2:c.237+255_237+256delinsAG	NP_001268421.1:n.237+255_237+256delinsAG
NM_001281493.2:c.-477+232_-477+233delinsAG	NP_001268422.1:n.-477+232_-477+233delinsAG