Canonical Allele Identifier: CA1229729462

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241870789_241870792delinsTTGA , CM000663.2:g.241870789_241870792delinsTTGA	GRCh38
NC_000001.10:g.242034091_242034094delinsTTGA , CM000663.1:g.242034091_242034094delinsTTGA	GRCh37
NC_000001.9:g.240100714_240100717delinsTTGA	NCBI36
NG_029100.1:g.27599_27602delinsTTGA
NG_029100.2:g.27599_27602delinsTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.1268-1243_1268-1240delinsTTGA MANE Select	ENSP00000355506.3:n.1268-1243_1268-1240delinsTTGA
ENST00000348581.9:c.1268-1243_1268-1240delinsTTGA	ENSP00000311873.5:n.1268-1243_1268-1240delinsTTGA
ENST00000366548.7:c.1268-1243_1268-1240delinsTTGA	ENSP00000355506.3:n.1268-1243_1268-1240delinsTTGA
ENST00000518483.5:c.1268-1243_1268-1240delinsTTGA	ENSP00000430251.1:n.1268-1243_1268-1240delinsTTGA
NM_003686.4:c.1268-1243_1268-1240delinsTTGA	NP_003677.4:n.1268-1243_1268-1240delinsTTGA
NM_006027.4:c.1268-1243_1268-1240delinsTTGA	NP_006018.4:n.1268-1243_1268-1240delinsTTGA
NM_130398.3:c.1268-1243_1268-1240delinsTTGA	NP_569082.2:n.1268-1243_1268-1240delinsTTGA
XM_005273350.2:c.1268-1246_1268-1243delinsTTGA	XP_005273407.1:n.1268-1246_1268-1243delinsTTGA
XM_006711840.1:c.1268-1243_1268-1240delinsTTGA	XP_006711903.1:n.1268-1243_1268-1240delinsTTGA
XM_011544321.1:c.1268-1243_1268-1240delinsTTGA	XP_011542623.1:n.1268-1243_1268-1240delinsTTGA
XM_011544322.1:c.1268-1243_1268-1240delinsTTGA	XP_011542624.1:n.1268-1243_1268-1240delinsTTGA
XM_011544323.1:c.1268-1246_1268-1243delinsTTGA	XP_011542625.1:n.1268-1246_1268-1243delinsTTGA
XM_011544324.1:c.1148-1243_1148-1240delinsTTGA	XP_011542626.1:n.1148-1243_1148-1240delinsTTGA
XM_011544325.1:c.305-1243_305-1240delinsTTGA	XP_011542627.1:n.305-1243_305-1240delinsTTGA
XM_011544326.1:c.1268-1243_1268-1240delinsTTGA	XP_011542628.1:n.1268-1243_1268-1240delinsTTGA
XR_949162.1:n.1853-1243_1853-1240delinsTTGA
NM_001319224.1:c.1268-1246_1268-1243delinsTTGA	NP_001306153.1:n.1268-1246_1268-1243delinsTTGA
XM_006711840.2:c.1268-1243_1268-1240delinsTTGA	XP_006711903.1:n.1268-1243_1268-1240delinsTTGA
XM_011544321.2:c.1268-1243_1268-1240delinsTTGA	XP_011542623.1:n.1268-1243_1268-1240delinsTTGA
XM_011544323.2:c.1268-1246_1268-1243delinsTTGA	XP_011542625.1:n.1268-1246_1268-1243delinsTTGA
XM_011544324.2:c.1148-1243_1148-1240delinsTTGA	XP_011542626.1:n.1148-1243_1148-1240delinsTTGA
XM_011544325.2:c.305-1243_305-1240delinsTTGA	XP_011542627.1:n.305-1243_305-1240delinsTTGA
XM_017002793.2:c.1148-1243_1148-1240delinsTTGA	XP_016858282.1:n.1148-1243_1148-1240delinsTTGA
NM_130398.4:c.1268-1243_1268-1240delinsTTGA MANE Select	NP_569082.2:n.1268-1243_1268-1240delinsTTGA
NM_001319224.2:c.1268-1246_1268-1243delinsTTGA	NP_001306153.1:n.1268-1246_1268-1243delinsTTGA