Canonical Allele Identifier: CA1229732271
Gene: EXO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241877514_241877515delinsAT , CM000663.2:g.241877514_241877515delinsAT GRCh38
NC_000001.10:g.242040816_242040817delinsAT , CM000663.1:g.242040816_242040817delinsAT GRCh37
NC_000001.9:g.240107439_240107440delinsAT NCBI36
NG_029100.1:g.34324_34325delinsAT
NG_029100.2:g.34324_34325delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000366548.8:c.1515-1235_1515-1234delinsAT MANE Select ENSP00000355506.3:n.1515-1235_1515-1234delinsAT
ENST00000348581.9:c.1515-1235_1515-1234delinsAT ENSP00000311873.5:n.1515-1235_1515-1234delinsAT
ENST00000366548.7:c.1515-1235_1515-1234delinsAT ENSP00000355506.3:n.1515-1235_1515-1234delinsAT
ENST00000518483.5:c.1515-1235_1515-1234delinsAT ENSP00000430251.1:n.1515-1235_1515-1234delinsAT
NM_003686.4:c.1515-1235_1515-1234delinsAT NP_003677.4:n.1515-1235_1515-1234delinsAT
NM_006027.4:c.1515-1235_1515-1234delinsAT NP_006018.4:n.1515-1235_1515-1234delinsAT
NM_130398.3:c.1515-1235_1515-1234delinsAT NP_569082.2:n.1515-1235_1515-1234delinsAT
XM_005273350.2:c.1512-1235_1512-1234delinsAT XP_005273407.1:n.1512-1235_1512-1234delinsAT
XM_006711840.1:c.1515-1235_1515-1234delinsAT XP_006711903.1:n.1515-1235_1515-1234delinsAT
XM_011544321.1:c.1515-1235_1515-1234delinsAT XP_011542623.1:n.1515-1235_1515-1234delinsAT
XM_011544322.1:c.1515-1235_1515-1234delinsAT XP_011542624.1:n.1515-1235_1515-1234delinsAT
XM_011544323.1:c.1512-1235_1512-1234delinsAT XP_011542625.1:n.1512-1235_1512-1234delinsAT
XM_011544324.1:c.1395-1235_1395-1234delinsAT XP_011542626.1:n.1395-1235_1395-1234delinsAT
XM_011544325.1:c.552-1235_552-1234delinsAT XP_011542627.1:n.552-1235_552-1234delinsAT
XM_011544326.1:c.1517-1236_1517-1235delinsAT XP_011542628.1:n.1517-1236_1517-1235delinsAT
XR_949162.1:n.2100-1235_2100-1234delinsAT
NM_001319224.1:c.1512-1235_1512-1234delinsAT NP_001306153.1:n.1512-1235_1512-1234delinsAT
XM_006711840.2:c.1515-1235_1515-1234delinsAT XP_006711903.1:n.1515-1235_1515-1234delinsAT
XM_011544321.2:c.1515-1235_1515-1234delinsAT XP_011542623.1:n.1515-1235_1515-1234delinsAT
XM_011544323.2:c.1512-1235_1512-1234delinsAT XP_011542625.1:n.1512-1235_1512-1234delinsAT
XM_011544324.2:c.1395-1235_1395-1234delinsAT XP_011542626.1:n.1395-1235_1395-1234delinsAT
XM_011544325.2:c.552-1235_552-1234delinsAT XP_011542627.1:n.552-1235_552-1234delinsAT
XM_017002793.2:c.1395-1235_1395-1234delinsAT XP_016858282.1:n.1395-1235_1395-1234delinsAT
NM_130398.4:c.1515-1235_1515-1234delinsAT MANE Select NP_569082.2:n.1515-1235_1515-1234delinsAT
NM_001319224.2:c.1512-1235_1512-1234delinsAT NP_001306153.1:n.1512-1235_1512-1234delinsAT