Canonical Allele Identifier: CA1229737355
Gene: EXO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241889746A= , CM000663.2:g.241889746A= GRCh38
NC_000001.10:g.242053048A= , CM000663.1:g.242053048A= GRCh37
NC_000001.9:g.240119671A= NCBI36
NG_029100.1:g.46556A=
NG_029100.2:g.46556A=

Transcript Alleles

HGVS Amino-acid change
ENST00000366548.8:c.*146A= MANE Select ENSP00000355506.3:n.*146A=
ENST00000348581.9:c.*146A= ENSP00000311873.5:n.*146A=
ENST00000366548.7:c.*146A= ENSP00000355506.3:n.*146A=
ENST00000518483.5:c.*273A= ENSP00000430251.1:n.*273A=
ENST00000518741.1:n.152-2778A=
NM_003686.4:c.*273A= NP_003677.4:n.*273A=
NM_006027.4:c.*146A= NP_006018.4:n.*146A=
NM_130398.3:c.*146A= NP_569082.2:n.*146A=
XM_005273350.2:c.*146A= XP_005273407.1:n.*146A=
XM_006711840.1:c.*146A= XP_006711903.1:n.*146A=
XM_011544321.1:c.*146A= XP_011542623.1:n.*146A=
XM_011544322.1:c.*146A= XP_011542624.1:n.*146A=
XM_011544323.1:c.*146A= XP_011542625.1:n.*146A=
XM_011544324.1:c.*146A= XP_011542626.1:n.*146A=
XM_011544325.1:c.*146A= XP_011542627.1:n.*146A=
XR_949162.1:n.2990+4239A=
NM_001319224.1:c.*146A= NP_001306153.1:n.*146A=
XM_006711840.2:c.*146A= XP_006711903.1:n.*146A=
XM_011544321.2:c.*146A= XP_011542623.1:n.*146A=
XM_011544323.2:c.*146A= XP_011542625.1:n.*146A=
XM_011544324.2:c.*146A= XP_011542626.1:n.*146A=
XM_011544325.2:c.*146A= XP_011542627.1:n.*146A=
XM_017002793.2:c.*146A= XP_016858282.1:n.*146A=
NM_130398.4:c.*146A= MANE Select NP_569082.2:n.*146A=
NM_001319224.2:c.*146A= NP_001306153.1:n.*146A=