Canonical Allele Identifier: CA1229737379

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241889827_241889828delinsGT , CM000663.2:g.241889827_241889828delinsGT	GRCh38
NC_000001.10:g.242053129_242053130delinsGT , CM000663.1:g.242053129_242053130delinsGT	GRCh37
NC_000001.9:g.240119752_240119753delinsGT	NCBI36
NG_029100.1:g.46637_46638delinsGT
NG_029100.2:g.46637_46638delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.*227_*228delinsGT MANE Select	ENSP00000355506.3:n.*227_*228delinsGT
ENST00000348581.9:c.*227_*228delinsGT	ENSP00000311873.5:n.*227_*228delinsGT
ENST00000366548.7:c.*227_*228delinsGT	ENSP00000355506.3:n.*227_*228delinsGT
ENST00000518741.1:n.152-2697_152-2696delinsGT
NM_003686.4:c.*354_*355delinsGT	NP_003677.4:n.*354_*355delinsGT
NM_006027.4:c.*227_*228delinsGT	NP_006018.4:n.*227_*228delinsGT
NM_130398.3:c.*227_*228delinsGT	NP_569082.2:n.*227_*228delinsGT
XM_011544321.1:c.*227_*228delinsGT	XP_011542623.1:n.*227_*228delinsGT
XM_011544322.1:c.*227_*228delinsGT	XP_011542624.1:n.*227_*228delinsGT
XR_949162.1:n.2990+4320_2990+4321delinsGT
NM_001319224.1:c.*227_*228delinsGT	NP_001306153.1:n.*227_*228delinsGT
XM_006711840.2:c.*227_*228delinsGT	XP_006711903.1:n.*227_*228delinsGT
XM_011544321.2:c.*227_*228delinsGT	XP_011542623.1:n.*227_*228delinsGT
XM_011544323.2:c.*227_*228delinsGT	XP_011542625.1:n.*227_*228delinsGT
XM_011544324.2:c.*227_*228delinsGT	XP_011542626.1:n.*227_*228delinsGT
XM_011544325.2:c.*227_*228delinsGT	XP_011542627.1:n.*227_*228delinsGT
XM_017002793.2:c.*227_*228delinsGT	XP_016858282.1:n.*227_*228delinsGT
NM_130398.4:c.*227_*228delinsGT MANE Select	NP_569082.2:n.*227_*228delinsGT
NM_001319224.2:c.*227_*228delinsGT	NP_001306153.1:n.*227_*228delinsGT