Canonical Allele Identifier: CA46716862

Linked Data

dbSNP Id: rs764772593

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47804726_47804727del , CM000664.2:g.47804726_47804727del GRCh38
NC_000002.11:g.48031865_48031866del , CM000664.1:g.48031865_48031866del GRCh37
NC_000002.10:g.47885369_47885370del NCBI36
NG_007111.1:g.26580_26581del , LRG_219:g.26580_26581del

Transcript Alleles

HGVS Amino-acid Change
ENST00000411819.2:c.3142-184_3142-183del (MSH6) ENSP00000406248.2:n.3142-184_3142-183del
ENST00000420813.6:c.3142-184_3142-183del (MSH6) ENSP00000390382.2:n.3142-184_3142-183del
ENST00000455383.6:c.3142-184_3142-183del (MSH6) ENSP00000397484.2:n.3142-184_3142-183del
ENST00000700004.2:c.3173-892_3173-891del (MSH6) ENSP00000514752.2:n.3173-892_3173-891del
ENST00000699999.1:n.3523-184_3523-183del (MSH6)
ENST00000700000.1:c.1873-184_1873-183del (MSH6) ENSP00000514749.1:n.1873-184_1873-183del
ENST00000700002.1:c.3445-184_3445-183del (MSH6) ENSP00000514750.1:n.3445-184_3445-183del
ENST00000700003.1:c.894-184_894-183del (MSH6) ENSP00000514751.1:n.894-184_894-183del
ENST00000700004.1:c.2330-892_2330-891del (MSH6) ENSP00000514752.1:n.2330-892_2330-891del
ENST00000700005.1:n.2290-184_2290-183del (MSH6)
ENST00000700006.1:n.3327_3328del (MSH6)
ENST00000700007.1:n.1444-184_1444-183del (MSH6)
ENST00000700008.1:n.1018-184_1018-183del (MSH6)
ENST00000700009.1:n.1017-184_1017-183del (MSH6)
ENST00000700010.1:n.848-184_848-183del (MSH6)
ENST00000700011.1:n.1959_1960del (MSH6)
ENST00000234420.11:c.3439-184_3439-183del (MSH6) MANE Select ENSP00000234420.5:n.3439-184_3439-183del
ENST00000540021.6:c.3049-184_3049-183del (MSH6) ENSP00000446475.1:n.3049-184_3049-183del
ENST00000652107.1:c.3142-184_3142-183del (MSH6) ENSP00000498629.1:n.3142-184_3142-183del
ENST00000673637.1:c.3142-184_3142-183del (MSH6) ENSP00000501310.1:n.3142-184_3142-183del
ENST00000234420.9:c.3439-184_3439-183del (MSH6) ENSP00000234420.4:n.3439-184_3439-183del
ENST00000405808.5:c.169+3468_169+3469del (FBXO11) ENSP00000385127.1:n.169+3468_169+3469del
ENST00000434234.5:c.*124+3267_*124+3268del (FBXO11) ENSP00000402692.1:n.*124+3267_*124+3268del
ENST00000445503.5:c.*2786-184_*2786-183del (MSH6) ENSP00000405294.1:n.*2786-184_*2786-183del
ENST00000538136.1:c.2533-184_2533-183del (MSH6) ENSP00000438580.1:n.2533-184_2533-183del
ENST00000540021.5:c.3049-184_3049-183del (MSH6) ENSP00000446475.1:n.3049-184_3049-183del
ENST00000614496.4:c.2533-184_2533-183del (MSH6) ENSP00000477844.1:n.2533-184_2533-183del
ENST00000622629.4:c.335-176_335-175del (MSH6) ENSP00000482078.1:n.335-176_335-175del
NM_000179.2:c.3439-184_3439-183del , LRG_219t1:c.3439-184_3439-183del (MSH6) NP_000170.1:n.3439-184_3439-183del
NM_001281492.1:c.3049-184_3049-183del (MSH6) NP_001268421.1:n.3049-184_3049-183del
NM_001281493.1:c.2533-184_2533-183del (MSH6) NP_001268422.1:n.2533-184_2533-183del
NM_001281494.1:c.2533-184_2533-183del (MSH6) NP_001268423.1:n.2533-184_2533-183del
XM_005264271.1:c.3142-184_3142-183del (MSH6) XP_005264328.1:n.3142-184_3142-183del
XM_011532798.1:c.3256-184_3256-183del (MSH6) XP_011531100.1:n.3256-184_3256-183del
XM_011532799.1:c.3142-184_3142-183del (MSH6) XP_011531101.1:n.3142-184_3142-183del
XM_011532800.1:c.3142-184_3142-183del (MSH6) XP_011531102.1:n.3142-184_3142-183del
XM_024452819.1:c.3439-184_3439-183del (MSH6) XP_024308587.1:n.3439-184_3439-183del
XM_024452820.1:c.3256-184_3256-183del (MSH6) XP_024308588.1:n.3256-184_3256-183del
XM_024452821.1:c.3142-184_3142-183del (MSH6) XP_024308589.1:n.3142-184_3142-183del
XM_024452822.1:c.2533-184_2533-183del (MSH6) XP_024308590.1:n.2533-184_2533-183del
NM_000179.3:c.3439-184_3439-183del (MSH6) MANE Select NP_000170.1:n.3439-184_3439-183del
NM_001281492.2:c.3049-184_3049-183del (MSH6) NP_001268421.1:n.3049-184_3049-183del
NM_001281493.2:c.2533-184_2533-183del (MSH6) NP_001268422.1:n.2533-184_2533-183del
NM_001281494.2:c.2533-184_2533-183del (MSH6) NP_001268423.1:n.2533-184_2533-183del