Canonical Allele Identifier: CA2496048483

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799165_47799167delinsTAC , CM000664.2:g.47799165_47799167delinsTAC	GRCh38
NC_000002.11:g.48026304_48026306delinsTAC , CM000664.1:g.48026304_48026306delinsTAC	GRCh37
NC_000002.10:g.47879808_47879810delinsTAC	NCBI36
NG_007111.1:g.21019_21021delinsTAC , LRG_219:g.21019_21021delinsTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.885_887delinsTAC (MSH6)	ENSP00000406248.2:p.Ser295=
ENST00000420813.6:c.885_887delinsTAC (MSH6)	ENSP00000390382.2:p.Ser295=
ENST00000455383.6:c.885_887delinsTAC (MSH6)	ENSP00000397484.2:p.Ser295=
ENST00000700004.2:c.1182_1184delinsTAC (MSH6)	ENSP00000514752.2:p.Ser394=
ENST00000699999.1:n.1266_1268delinsTAC (MSH6)
ENST00000700000.1:c.1182_1184delinsTAC (MSH6)	ENSP00000514749.1:p.Ser394=
ENST00000700002.1:c.1188_1190delinsTAC (MSH6)	ENSP00000514750.1:p.Ser396=
ENST00000700003.1:c.627+3102_627+3104delinsTAC (MSH6)	ENSP00000514751.1:n.627+3102_627+3104delinsTAC
ENST00000700004.1:c.339_341delinsTAC (MSH6)	ENSP00000514752.1:p.Ser113=
ENST00000234420.11:c.1182_1184delinsTAC (MSH6) MANE Select	ENSP00000234420.5:p.Ser394=
ENST00000540021.6:c.792_794delinsTAC (MSH6)	ENSP00000446475.1:p.Ser264=
ENST00000652107.1:c.885_887delinsTAC (MSH6)	ENSP00000498629.1:p.Ser295=
ENST00000673637.1:c.885_887delinsTAC (MSH6)	ENSP00000501310.1:p.Ser295=
ENST00000234420.9:c.1182_1184delinsTAC (MSH6)	ENSP00000234420.4:p.Ser394=
ENST00000405808.5:c.169+9028_169+9030delinsGTA (FBXO11)	ENSP00000385127.1:n.169+9028_169+9030delinsGTA
ENST00000434234.5:c.*124+8827_*124+8829delinsGTA (FBXO11)	ENSP00000402692.1:n.*124+8827_*124+8829delinsGTA
ENST00000445503.5:c.*529_*531delinsTAC (MSH6)	ENSP00000405294.1:n.*529_*531delinsTAC
ENST00000538136.1:c.276_278delinsTAC (MSH6)	ENSP00000438580.1:p.Ser92=
ENST00000540021.5:c.792_794delinsTAC (MSH6)	ENSP00000446475.1:p.Ser264=
ENST00000614496.4:c.276_278delinsTAC (MSH6)	ENSP00000477844.1:p.Ser92=
ENST00000616033.4:c.1179_1181delinsTAC (MSH6)	ENSP00000480261.1:p.Ser393=
ENST00000622629.4:c.-1915_-1913delinsTAC (MSH6)	ENSP00000482078.1:n.-1915_-1913delinsTAC
NM_000179.2:c.1182_1184delinsTAC , LRG_219t1:c.1182_1184delinsTAC (MSH6)	NP_000170.1:p.Ser394=
NM_001281492.1:c.792_794delinsTAC (MSH6)	NP_001268421.1:p.Ser264=
NM_001281493.1:c.276_278delinsTAC (MSH6)	NP_001268422.1:p.Ser92=
NM_001281494.1:c.276_278delinsTAC (MSH6)	NP_001268423.1:p.Ser92=
XM_005264271.1:c.885_887delinsTAC (MSH6)	XP_005264328.1:p.Ser295=
XM_011532798.1:c.999_1001delinsTAC (MSH6)	XP_011531100.1:p.Ser333=
XM_011532799.1:c.885_887delinsTAC (MSH6)	XP_011531101.1:p.Ser295=
XM_011532800.1:c.885_887delinsTAC (MSH6)	XP_011531102.1:p.Ser295=
XM_024452819.1:c.1182_1184delinsTAC (MSH6)	XP_024308587.1:p.Ser394=
XM_024452820.1:c.999_1001delinsTAC (MSH6)	XP_024308588.1:p.Ser333=
XM_024452821.1:c.885_887delinsTAC (MSH6)	XP_024308589.1:p.Ser295=
XM_024452822.1:c.276_278delinsTAC (MSH6)	XP_024308590.1:p.Ser92=
NM_000179.3:c.1182_1184delinsTAC (MSH6) MANE Select	NP_000170.1:p.Ser394=
NM_001281492.2:c.792_794delinsTAC (MSH6)	NP_001268421.1:p.Ser264=
NM_001281493.2:c.276_278delinsTAC (MSH6)	NP_001268422.1:p.Ser92=
NM_001281494.2:c.276_278delinsTAC (MSH6)	NP_001268423.1:p.Ser92=