Canonical Allele Identifier: CA1229732224

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241877445_241877446delinsGA , CM000663.2:g.241877445_241877446delinsGA	GRCh38
NC_000001.10:g.242040747_242040748delinsGA , CM000663.1:g.242040747_242040748delinsGA	GRCh37
NC_000001.9:g.240107370_240107371delinsGA	NCBI36
NG_029100.1:g.34255_34256delinsGA
NG_029100.2:g.34255_34256delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.1515-1304_1515-1303delinsGA MANE Select	ENSP00000355506.3:n.1515-1304_1515-1303delinsGA
ENST00000348581.9:c.1515-1304_1515-1303delinsGA	ENSP00000311873.5:n.1515-1304_1515-1303delinsGA
ENST00000366548.7:c.1515-1304_1515-1303delinsGA	ENSP00000355506.3:n.1515-1304_1515-1303delinsGA
ENST00000518483.5:c.1515-1304_1515-1303delinsGA	ENSP00000430251.1:n.1515-1304_1515-1303delinsGA
NM_003686.4:c.1515-1304_1515-1303delinsGA	NP_003677.4:n.1515-1304_1515-1303delinsGA
NM_006027.4:c.1515-1304_1515-1303delinsGA	NP_006018.4:n.1515-1304_1515-1303delinsGA
NM_130398.3:c.1515-1304_1515-1303delinsGA	NP_569082.2:n.1515-1304_1515-1303delinsGA
XM_005273350.2:c.1512-1304_1512-1303delinsGA	XP_005273407.1:n.1512-1304_1512-1303delinsGA
XM_006711840.1:c.1515-1304_1515-1303delinsGA	XP_006711903.1:n.1515-1304_1515-1303delinsGA
XM_011544321.1:c.1515-1304_1515-1303delinsGA	XP_011542623.1:n.1515-1304_1515-1303delinsGA
XM_011544322.1:c.1515-1304_1515-1303delinsGA	XP_011542624.1:n.1515-1304_1515-1303delinsGA
XM_011544323.1:c.1512-1304_1512-1303delinsGA	XP_011542625.1:n.1512-1304_1512-1303delinsGA
XM_011544324.1:c.1395-1304_1395-1303delinsGA	XP_011542626.1:n.1395-1304_1395-1303delinsGA
XM_011544325.1:c.552-1304_552-1303delinsGA	XP_011542627.1:n.552-1304_552-1303delinsGA
XM_011544326.1:c.1517-1305_1517-1304delinsGA	XP_011542628.1:n.1517-1305_1517-1304delinsGA
XR_949162.1:n.2100-1304_2100-1303delinsGA
NM_001319224.1:c.1512-1304_1512-1303delinsGA	NP_001306153.1:n.1512-1304_1512-1303delinsGA
XM_006711840.2:c.1515-1304_1515-1303delinsGA	XP_006711903.1:n.1515-1304_1515-1303delinsGA
XM_011544321.2:c.1515-1304_1515-1303delinsGA	XP_011542623.1:n.1515-1304_1515-1303delinsGA
XM_011544323.2:c.1512-1304_1512-1303delinsGA	XP_011542625.1:n.1512-1304_1512-1303delinsGA
XM_011544324.2:c.1395-1304_1395-1303delinsGA	XP_011542626.1:n.1395-1304_1395-1303delinsGA
XM_011544325.2:c.552-1304_552-1303delinsGA	XP_011542627.1:n.552-1304_552-1303delinsGA
XM_017002793.2:c.1395-1304_1395-1303delinsGA	XP_016858282.1:n.1395-1304_1395-1303delinsGA
NM_130398.4:c.1515-1304_1515-1303delinsGA MANE Select	NP_569082.2:n.1515-1304_1515-1303delinsGA
NM_001319224.2:c.1512-1304_1512-1303delinsGA	NP_001306153.1:n.1512-1304_1512-1303delinsGA