Canonical Allele Identifier: CA40371073
Gene: EXO1 HGNC NCBI

Linked Data

dbSNP Id: rs72755295

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241870961A>G , CM000663.2:g.241870961A>G GRCh38
NC_000001.10:g.242034263A>G , CM000663.1:g.242034263A>G GRCh37
NC_000001.9:g.240100886A>G NCBI36
NG_029100.1:g.27771A>G
NG_029100.2:g.27771A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366548.8:c.1268-1071A>G MANE Select ENSP00000355506.3:n.1268-1071A>G
ENST00000348581.9:c.1268-1071A>G ENSP00000311873.5:n.1268-1071A>G
ENST00000366548.7:c.1268-1071A>G ENSP00000355506.3:n.1268-1071A>G
ENST00000518483.5:c.1268-1071A>G ENSP00000430251.1:n.1268-1071A>G
NM_003686.4:c.1268-1071A>G NP_003677.4:n.1268-1071A>G
NM_006027.4:c.1268-1071A>G NP_006018.4:n.1268-1071A>G
NM_130398.3:c.1268-1071A>G NP_569082.2:n.1268-1071A>G
XM_005273350.2:c.1268-1074A>G XP_005273407.1:n.1268-1074A>G
XM_006711840.1:c.1268-1071A>G XP_006711903.1:n.1268-1071A>G
XM_011544321.1:c.1268-1071A>G XP_011542623.1:n.1268-1071A>G
XM_011544322.1:c.1268-1071A>G XP_011542624.1:n.1268-1071A>G
XM_011544323.1:c.1268-1074A>G XP_011542625.1:n.1268-1074A>G
XM_011544324.1:c.1148-1071A>G XP_011542626.1:n.1148-1071A>G
XM_011544325.1:c.305-1071A>G XP_011542627.1:n.305-1071A>G
XM_011544326.1:c.1268-1071A>G XP_011542628.1:n.1268-1071A>G
XR_949162.1:n.1853-1071A>G
NM_001319224.1:c.1268-1074A>G NP_001306153.1:n.1268-1074A>G
XM_006711840.2:c.1268-1071A>G XP_006711903.1:n.1268-1071A>G
XM_011544321.2:c.1268-1071A>G XP_011542623.1:n.1268-1071A>G
XM_011544323.2:c.1268-1074A>G XP_011542625.1:n.1268-1074A>G
XM_011544324.2:c.1148-1071A>G XP_011542626.1:n.1148-1071A>G
XM_011544325.2:c.305-1071A>G XP_011542627.1:n.305-1071A>G
XM_017002793.2:c.1148-1071A>G XP_016858282.1:n.1148-1071A>G
NM_130398.4:c.1268-1071A>G MANE Select NP_569082.2:n.1268-1071A>G
NM_001319224.2:c.1268-1074A>G NP_001306153.1:n.1268-1074A>G