Canonical Allele Identifier: CA2651276773
Gene: EXO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241889894del , CM000663.2:g.241889894del GRCh38
NC_000001.10:g.242053196del , CM000663.1:g.242053196del GRCh37
NC_000001.9:g.240119819del NCBI36
NG_029100.1:g.46704del
NG_029100.2:g.46704del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366548.8:c.*294del MANE Select ENSP00000355506.3:n.*294del
ENST00000348581.9:c.*294del ENSP00000311873.5:n.*294del
ENST00000366548.7:c.*294del ENSP00000355506.3:n.*294del
ENST00000518741.1:n.152-2630del
NM_003686.4:c.*421del NP_003677.4:n.*421del
NM_006027.4:c.*294del NP_006018.4:n.*294del
NM_130398.3:c.*294del NP_569082.2:n.*294del
XM_011544321.1:c.*294del XP_011542623.1:n.*294del
XM_011544322.1:c.*294del XP_011542624.1:n.*294del
XR_949162.1:n.2990+4387del
NM_001319224.1:c.*294del NP_001306153.1:n.*294del
XM_006711840.2:c.*294del XP_006711903.1:n.*294del
XM_011544321.2:c.*294del XP_011542623.1:n.*294del
XM_011544323.2:c.*294del XP_011542625.1:n.*294del
XM_011544324.2:c.*294del XP_011542626.1:n.*294del
XM_011544325.2:c.*294del XP_011542627.1:n.*294del
XM_017002793.2:c.*294del XP_016858282.1:n.*294del
NM_130398.4:c.*294del MANE Select NP_569082.2:n.*294del
NM_001319224.2:c.*294del NP_001306153.1:n.*294del