Canonical Allele Identifier: CA2658966071

Gene: MSH6

Linked Data

• gnomAD v4: 2-47783595-T-TTA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783595_47783596insTA , CM000664.2:g.47783595_47783596insTA	GRCh38
NC_000002.11:g.48010734_48010735insTA , CM000664.1:g.48010734_48010735insTA	GRCh37
NC_000002.10:g.47864238_47864239insTA	NCBI36
NG_007111.1:g.5449_5450insTA , LRG_219:g.5449_5450insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455383.6:c.-221_-220insTA	ENSP00000397484.2:n.-221_-220insTA
ENST00000700004.2:c.260+102_260+103insTA	ENSP00000514752.2:n.260+102_260+103insTA
ENST00000699999.1:n.344+102_344+103insTA
ENST00000700000.1:c.260+102_260+103insTA	ENSP00000514749.1:n.260+102_260+103insTA
ENST00000700001.1:n.332+102_332+103insTA
ENST00000700002.1:c.260+102_260+103insTA	ENSP00000514750.1:n.260+102_260+103insTA
ENST00000700003.1:c.260+102_260+103insTA	ENSP00000514751.1:n.260+102_260+103insTA
ENST00000234420.11:c.260+102_260+103insTA MANE Select	ENSP00000234420.5:n.260+102_260+103insTA
ENST00000540021.6:c.237+125_237+126insTA	ENSP00000446475.1:n.237+125_237+126insTA
ENST00000652107.1:c.-37-7332_-37-7331insTA	ENSP00000498629.1:n.-37-7332_-37-7331insTA
ENST00000673637.1:c.-38+364_-38+365insTA	ENSP00000501310.1:n.-38+364_-38+365insTA
ENST00000673922.1:n.349+102_349+103insTA
ENST00000234420.9:c.260+102_260+103insTA	ENSP00000234420.4:n.260+102_260+103insTA
ENST00000445503.5:c.260+102_260+103insTA	ENSP00000405294.1:n.260+102_260+103insTA
ENST00000455383.5:c.-221_-220insTA	ENSP00000397484.1:n.-221_-220insTA
ENST00000456246.1:c.260+102_260+103insTA	ENSP00000410570.1:n.260+102_260+103insTA
ENST00000493177.1:n.324+102_324+103insTA
ENST00000540021.5:c.237+125_237+126insTA	ENSP00000446475.1:n.237+125_237+126insTA
ENST00000606499.1:c.-37-7332_-37-7331insTA	ENSP00000475605.1:n.-37-7332_-37-7331insTA
ENST00000614496.4:c.-477+102_-477+103insTA	ENSP00000477844.1:n.-477+102_-477+103insTA
ENST00000616033.4:c.257+102_257+103insTA	ENSP00000480261.1:n.257+102_257+103insTA
ENST00000622629.4:c.-2837+102_-2837+103insTA	ENSP00000482078.1:n.-2837+102_-2837+103insTA
NM_000179.2:c.260+102_260+103insTA , LRG_219t1:c.260+102_260+103insTA	NP_000170.1:n.260+102_260+103insTA
NM_001281492.1:c.237+125_237+126insTA	NP_001268421.1:n.237+125_237+126insTA
NM_001281493.1:c.-477+102_-477+103insTA	NP_001268422.1:n.-477+102_-477+103insTA
XM_011532799.1:c.-221_-220insTA	XP_011531101.1:n.-221_-220insTA
XM_011532800.1:c.-38+364_-38+365insTA	XP_011531102.1:n.-38+364_-38+365insTA
XM_024452819.1:c.260+102_260+103insTA	XP_024308587.1:n.260+102_260+103insTA
XM_024452821.1:c.-221_-220insTA	XP_024308589.1:n.-221_-220insTA
XM_024452822.1:c.-477+102_-477+103insTA	XP_024308590.1:n.-477+102_-477+103insTA
NM_000179.3:c.260+102_260+103insTA MANE Select	NP_000170.1:n.260+102_260+103insTA
NM_001281492.2:c.237+125_237+126insTA	NP_001268421.1:n.237+125_237+126insTA
NM_001281493.2:c.-477+102_-477+103insTA	NP_001268422.1:n.-477+102_-477+103insTA