Canonical Allele Identifier: CA2699117028

Linked Data

dbSNP Id: rs1433876323

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806405C>A , CM000664.2:g.47806405C>A GRCh38
NC_000002.11:g.48033544C>A , CM000664.1:g.48033544C>A GRCh37
NC_000002.10:g.47887048C>A NCBI36
NG_007111.1:g.28259C>A , LRG_219:g.28259C>A
NG_008397.1:g.104271G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3505-47C>A (MSH6) ENSP00000406248.2:n.3505-47C>A
ENST00000420813.6:c.3505-47C>A (MSH6) ENSP00000390382.2:n.3505-47C>A
ENST00000455383.6:c.3505-47C>A (MSH6) ENSP00000397484.2:n.3505-47C>A
ENST00000700004.2:c.3418-47C>A (MSH6) ENSP00000514752.2:n.3418-47C>A
ENST00000699999.1:n.4476-47C>A (MSH6)
ENST00000700000.1:c.2236-47C>A (MSH6) ENSP00000514749.1:n.2236-47C>A
ENST00000700002.1:c.3808-47C>A (MSH6) ENSP00000514750.1:n.3808-47C>A
ENST00000700003.1:c.1257-47C>A (MSH6) ENSP00000514751.1:n.1257-47C>A
ENST00000700004.1:c.2575-47C>A (MSH6) ENSP00000514752.1:n.2575-47C>A
ENST00000700005.1:n.2653-47C>A (MSH6)
ENST00000700006.1:n.4960-47C>A (MSH6)
ENST00000700007.1:n.2397-47C>A (MSH6)
ENST00000700008.1:n.2017C>A (MSH6)
ENST00000700009.1:n.2466-47C>A (MSH6)
ENST00000700010.1:n.1211-47C>A (MSH6)
ENST00000700011.1:n.3096-47C>A (MSH6)
ENST00000682451.1:n.4343G>T (FBXO11)
ENST00000684712.1:n.4605G>T (FBXO11)
ENST00000234420.11:c.3802-47C>A (MSH6) MANE Select ENSP00000234420.5:n.3802-47C>A
ENST00000540021.6:c.3412-47C>A (MSH6) ENSP00000446475.1:n.3412-47C>A
ENST00000652107.1:c.3505-47C>A (MSH6) ENSP00000498629.1:n.3505-47C>A
ENST00000673637.1:c.3505-47C>A (MSH6) ENSP00000501310.1:n.3505-47C>A
ENST00000234420.9:c.3802-47C>A (MSH6) ENSP00000234420.4:n.3802-47C>A
ENST00000405808.5:c.169+1790G>T (FBXO11) ENSP00000385127.1:n.169+1790G>T
ENST00000434234.5:c.*124+1589G>T (FBXO11) ENSP00000402692.1:n.*124+1589G>T
ENST00000445503.5:c.*3149-47C>A (MSH6) ENSP00000405294.1:n.*3149-47C>A
ENST00000538136.1:c.2896-47C>A (MSH6) ENSP00000438580.1:n.2896-47C>A
ENST00000540021.5:c.3412-47C>A (MSH6) ENSP00000446475.1:n.3412-47C>A
ENST00000614496.4:c.2896-47C>A (MSH6) ENSP00000477844.1:n.2896-47C>A
ENST00000622629.4:c.703-47C>A (MSH6) ENSP00000482078.1:n.703-47C>A
NM_000179.2:c.3802-47C>A , LRG_219t1:c.3802-47C>A (MSH6) NP_000170.1:n.3802-47C>A
NM_001281492.1:c.3412-47C>A (MSH6) NP_001268421.1:n.3412-47C>A
NM_001281493.1:c.2896-47C>A (MSH6) NP_001268422.1:n.2896-47C>A
NM_001281494.1:c.2896-47C>A (MSH6) NP_001268423.1:n.2896-47C>A
XM_005264271.1:c.3505-47C>A (MSH6) XP_005264328.1:n.3505-47C>A
XM_011532798.1:c.3619-47C>A (MSH6) XP_011531100.1:n.3619-47C>A
XM_011532799.1:c.3505-47C>A (MSH6) XP_011531101.1:n.3505-47C>A
XM_011532800.1:c.3505-47C>A (MSH6) XP_011531102.1:n.3505-47C>A
XM_024452819.1:c.3848C>A (MSH6) XP_024308587.1:p.Ala1283Glu
XM_024452820.1:c.3665C>A (MSH6) XP_024308588.1:p.Ala1222Glu
XM_024452821.1:c.3551C>A (MSH6) XP_024308589.1:p.Ala1184Glu
XM_024452822.1:c.2942C>A (MSH6) XP_024308590.1:p.Ala981Glu
NM_000179.3:c.3802-47C>A (MSH6) MANE Select NP_000170.1:n.3802-47C>A
NM_001281492.2:c.3412-47C>A (MSH6) NP_001268421.1:n.3412-47C>A
NM_001281493.2:c.2896-47C>A (MSH6) NP_001268422.1:n.2896-47C>A
NM_001281494.2:c.2896-47C>A (MSH6) NP_001268423.1:n.2896-47C>A