Canonical Allele Identifier: CA2496049353

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800333_47800335delinsAAC , CM000664.2:g.47800333_47800335delinsAAC	GRCh38
NC_000002.11:g.48027472_48027474delinsAAC , CM000664.1:g.48027472_48027474delinsAAC	GRCh37
NC_000002.10:g.47880976_47880978delinsAAC	NCBI36
NG_007111.1:g.22187_22189delinsAAC , LRG_219:g.22187_22189delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2053_2055delinsAAC (MSH6)	ENSP00000406248.2:p.Asn685=
ENST00000420813.6:c.2053_2055delinsAAC (MSH6)	ENSP00000390382.2:p.Asn685=
ENST00000455383.6:c.2053_2055delinsAAC (MSH6)	ENSP00000397484.2:p.Asn685=
ENST00000700004.2:c.2350_2352delinsAAC (MSH6)	ENSP00000514752.2:p.Asn784=
ENST00000699999.1:n.2434_2436delinsAAC (MSH6)
ENST00000700000.1:c.1606+744_1606+746delinsAAC (MSH6)	ENSP00000514749.1:n.1606+744_1606+746delinsAAC
ENST00000700002.1:c.2356_2358delinsAAC (MSH6)	ENSP00000514750.1:p.Asn786=
ENST00000700003.1:c.628-3087_628-3085delinsAAC (MSH6)	ENSP00000514751.1:n.628-3087_628-3085delinsAAC
ENST00000700004.1:c.1507_1509delinsAAC (MSH6)	ENSP00000514752.1:p.Asn503=
ENST00000234420.11:c.2350_2352delinsAAC (MSH6) MANE Select	ENSP00000234420.5:p.Asn784=
ENST00000540021.6:c.1960_1962delinsAAC (MSH6)	ENSP00000446475.1:p.Asn654=
ENST00000652107.1:c.2053_2055delinsAAC (MSH6)	ENSP00000498629.1:p.Asn685=
ENST00000673637.1:c.2053_2055delinsAAC (MSH6)	ENSP00000501310.1:p.Asn685=
ENST00000234420.9:c.2350_2352delinsAAC (MSH6)	ENSP00000234420.4:p.Asn784=
ENST00000405808.5:c.169+7860_169+7862delinsGTT (FBXO11)	ENSP00000385127.1:n.169+7860_169+7862delinsGTT
ENST00000434234.5:c.*124+7659_*124+7661delinsGTT (FBXO11)	ENSP00000402692.1:n.*124+7659_*124+7661delinsGTT
ENST00000445503.5:c.*1697_*1699delinsAAC (MSH6)	ENSP00000405294.1:n.*1697_*1699delinsAAC
ENST00000538136.1:c.1444_1446delinsAAC (MSH6)	ENSP00000438580.1:p.Asn482=
ENST00000540021.5:c.1960_1962delinsAAC (MSH6)	ENSP00000446475.1:p.Asn654=
ENST00000614496.4:c.1444_1446delinsAAC (MSH6)	ENSP00000477844.1:p.Asn482=
ENST00000616033.4:c.2347_2349delinsAAC (MSH6)	ENSP00000480261.1:p.Asn783=
ENST00000622629.4:c.-747_-745delinsAAC (MSH6)	ENSP00000482078.1:n.-747_-745delinsAAC
NM_000179.2:c.2350_2352delinsAAC , LRG_219t1:c.2350_2352delinsAAC (MSH6)	NP_000170.1:p.Asn784=
NM_001281492.1:c.1960_1962delinsAAC (MSH6)	NP_001268421.1:p.Asn654=
NM_001281493.1:c.1444_1446delinsAAC (MSH6)	NP_001268422.1:p.Asn482=
NM_001281494.1:c.1444_1446delinsAAC (MSH6)	NP_001268423.1:p.Asn482=
XM_005264271.1:c.2053_2055delinsAAC (MSH6)	XP_005264328.1:p.Asn685=
XM_011532798.1:c.2167_2169delinsAAC (MSH6)	XP_011531100.1:p.Asn723=
XM_011532799.1:c.2053_2055delinsAAC (MSH6)	XP_011531101.1:p.Asn685=
XM_011532800.1:c.2053_2055delinsAAC (MSH6)	XP_011531102.1:p.Asn685=
XM_024452819.1:c.2350_2352delinsAAC (MSH6)	XP_024308587.1:p.Asn784=
XM_024452820.1:c.2167_2169delinsAAC (MSH6)	XP_024308588.1:p.Asn723=
XM_024452821.1:c.2053_2055delinsAAC (MSH6)	XP_024308589.1:p.Asn685=
XM_024452822.1:c.1444_1446delinsAAC (MSH6)	XP_024308590.1:p.Asn482=
NM_000179.3:c.2350_2352delinsAAC (MSH6) MANE Select	NP_000170.1:p.Asn784=
NM_001281492.2:c.1960_1962delinsAAC (MSH6)	NP_001268421.1:p.Asn654=
NM_001281493.2:c.1444_1446delinsAAC (MSH6)	NP_001268422.1:p.Asn482=
NM_001281494.2:c.1444_1446delinsAAC (MSH6)	NP_001268423.1:p.Asn482=