Canonical Allele Identifier: CA769464177

Linked Data

dbSNP Id: rs1409877477

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47805488_47805489del , CM000664.2:g.47805488_47805489del GRCh38
NC_000002.11:g.48032627_48032628del , CM000664.1:g.48032627_48032628del GRCh37
NC_000002.10:g.47886131_47886132del NCBI36
NG_007111.1:g.27342_27343del , LRG_219:g.27342_27343del
NG_008397.1:g.105188_105189del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3260-130_3260-129del (MSH6) ENSP00000406248.2:n.3260-130_3260-129del
ENST00000420813.6:c.3260-130_3260-129del (MSH6) ENSP00000390382.2:n.3260-130_3260-129del
ENST00000455383.6:c.3260-130_3260-129del (MSH6) ENSP00000397484.2:n.3260-130_3260-129del
ENST00000700004.2:c.3173-130_3173-129del (MSH6) ENSP00000514752.2:n.3173-130_3173-129del
ENST00000699999.1:n.4101_4102del (MSH6)
ENST00000700000.1:c.1991-130_1991-129del (MSH6) ENSP00000514749.1:n.1991-130_1991-129del
ENST00000700002.1:c.3563-130_3563-129del (MSH6) ENSP00000514750.1:n.3563-130_3563-129del
ENST00000700003.1:c.1012-130_1012-129del (MSH6) ENSP00000514751.1:n.1012-130_1012-129del
ENST00000700004.1:c.2330-130_2330-129del (MSH6) ENSP00000514752.1:n.2330-130_2330-129del
ENST00000700005.1:n.2408-130_2408-129del (MSH6)
ENST00000700006.1:n.4089_4090del (MSH6)
ENST00000700007.1:n.2022_2023del (MSH6)
ENST00000700008.1:n.1596_1597del (MSH6)
ENST00000700009.1:n.1595_1596del (MSH6)
ENST00000700010.1:n.966-130_966-129del (MSH6)
ENST00000700011.1:n.2721_2722del (MSH6)
ENST00000234420.11:c.3557-130_3557-129del (MSH6) MANE Select ENSP00000234420.5:n.3557-130_3557-129del
ENST00000540021.6:c.3167-130_3167-129del (MSH6) ENSP00000446475.1:n.3167-130_3167-129del
ENST00000652107.1:c.3260-130_3260-129del (MSH6) ENSP00000498629.1:n.3260-130_3260-129del
ENST00000673637.1:c.3260-130_3260-129del (MSH6) ENSP00000501310.1:n.3260-130_3260-129del
ENST00000234420.9:c.3557-130_3557-129del (MSH6) ENSP00000234420.4:n.3557-130_3557-129del
ENST00000405808.5:c.169+2707_169+2708del (FBXO11) ENSP00000385127.1:n.169+2707_169+2708del
ENST00000434234.5:c.*124+2506_*124+2507del (FBXO11) ENSP00000402692.1:n.*124+2506_*124+2507de...
ENST00000445503.5:c.*2904-130_*2904-129del (MSH6) ENSP00000405294.1:n.*2904-130_*2904-129de...
ENST00000538136.1:c.2651-130_2651-129del (MSH6) ENSP00000438580.1:n.2651-130_2651-129del
ENST00000540021.5:c.3167-130_3167-129del (MSH6) ENSP00000446475.1:n.3167-130_3167-129del
ENST00000614496.4:c.2651-130_2651-129del (MSH6) ENSP00000477844.1:n.2651-130_2651-129del
ENST00000622629.4:c.461-130_461-129del (MSH6) ENSP00000482078.1:n.461-130_461-129del
NM_000179.2:c.3557-130_3557-129del , LRG_219t1:c.3557-130_3557-129del (MSH6) NP_000170.1:n.3557-130_3557-129del
NM_001281492.1:c.3167-130_3167-129del (MSH6) NP_001268421.1:n.3167-130_3167-129del
NM_001281493.1:c.2651-130_2651-129del (MSH6) NP_001268422.1:n.2651-130_2651-129del
NM_001281494.1:c.2651-130_2651-129del (MSH6) NP_001268423.1:n.2651-130_2651-129del
XM_005264271.1:c.3260-130_3260-129del (MSH6) XP_005264328.1:n.3260-130_3260-129del
XM_011532798.1:c.3374-130_3374-129del (MSH6) XP_011531100.1:n.3374-130_3374-129del
XM_011532799.1:c.3260-130_3260-129del (MSH6) XP_011531101.1:n.3260-130_3260-129del
XM_011532800.1:c.3260-130_3260-129del (MSH6) XP_011531102.1:n.3260-130_3260-129del
XM_024452819.1:c.3557-130_3557-129del (MSH6) XP_024308587.1:n.3557-130_3557-129del
XM_024452820.1:c.3374-130_3374-129del (MSH6) XP_024308588.1:n.3374-130_3374-129del
XM_024452821.1:c.3260-130_3260-129del (MSH6) XP_024308589.1:n.3260-130_3260-129del
XM_024452822.1:c.2651-130_2651-129del (MSH6) XP_024308590.1:n.2651-130_2651-129del
NM_000179.3:c.3557-130_3557-129del (MSH6) MANE Select NP_000170.1:n.3557-130_3557-129del
NM_001281492.2:c.3167-130_3167-129del (MSH6) NP_001268421.1:n.3167-130_3167-129del
NM_001281493.2:c.2651-130_2651-129del (MSH6) NP_001268422.1:n.2651-130_2651-129del
NM_001281494.2:c.2651-130_2651-129del (MSH6) NP_001268423.1:n.2651-130_2651-129del