Canonical Allele Identifier: CA1014043024
Gene: EXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1662039525

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241870794dup , CM000663.2:g.241870794dup GRCh38
NC_000001.10:g.242034096dup , CM000663.1:g.242034096dup GRCh37
NC_000001.9:g.240100719dup NCBI36
NG_029100.1:g.27604dup
NG_029100.2:g.27604dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000366548.8:c.1268-1238dup MANE Select ENSP00000355506.3:n.1268-1238dup
ENST00000348581.9:c.1268-1238dup ENSP00000311873.5:n.1268-1238dup
ENST00000366548.7:c.1268-1238dup ENSP00000355506.3:n.1268-1238dup
ENST00000518483.5:c.1268-1238dup ENSP00000430251.1:n.1268-1238dup
NM_003686.4:c.1268-1238dup NP_003677.4:n.1268-1238dup
NM_006027.4:c.1268-1238dup NP_006018.4:n.1268-1238dup
NM_130398.3:c.1268-1238dup NP_569082.2:n.1268-1238dup
XM_005273350.2:c.1268-1241dup XP_005273407.1:n.1268-1241dup
XM_006711840.1:c.1268-1238dup XP_006711903.1:n.1268-1238dup
XM_011544321.1:c.1268-1238dup XP_011542623.1:n.1268-1238dup
XM_011544322.1:c.1268-1238dup XP_011542624.1:n.1268-1238dup
XM_011544323.1:c.1268-1241dup XP_011542625.1:n.1268-1241dup
XM_011544324.1:c.1148-1238dup XP_011542626.1:n.1148-1238dup
XM_011544325.1:c.305-1238dup XP_011542627.1:n.305-1238dup
XM_011544326.1:c.1268-1238dup XP_011542628.1:n.1268-1238dup
XR_949162.1:n.1853-1238dup
NM_001319224.1:c.1268-1241dup NP_001306153.1:n.1268-1241dup
XM_006711840.2:c.1268-1238dup XP_006711903.1:n.1268-1238dup
XM_011544321.2:c.1268-1238dup XP_011542623.1:n.1268-1238dup
XM_011544323.2:c.1268-1241dup XP_011542625.1:n.1268-1241dup
XM_011544324.2:c.1148-1238dup XP_011542626.1:n.1148-1238dup
XM_011544325.2:c.305-1238dup XP_011542627.1:n.305-1238dup
XM_017002793.2:c.1148-1238dup XP_016858282.1:n.1148-1238dup
NM_130398.4:c.1268-1238dup MANE Select NP_569082.2:n.1268-1238dup
NM_001319224.2:c.1268-1241dup NP_001306153.1:n.1268-1241dup