Canonical Allele Identifier: CA646707779

Gene: EXO1

Linked Data

• gnomAD v4: 1-241889760-GT-G
• COSMIC: COSN18724482

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241889767del , CM000663.2:g.241889767del	GRCh38
NC_000001.10:g.242053069del , CM000663.1:g.242053069del	GRCh37
NC_000001.9:g.240119692del	NCBI36
NG_029100.1:g.46577del
NG_029100.2:g.46577del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.*167del MANE Select	ENSP00000355506.3:n.*167del
ENST00000348581.9:c.*167del	ENSP00000311873.5:n.*167del
ENST00000366548.7:c.*167del	ENSP00000355506.3:n.*167del
ENST00000518741.1:n.152-2757del
NM_003686.4:c.*294del	NP_003677.4:n.*294del
NM_006027.4:c.*167del	NP_006018.4:n.*167del
NM_130398.3:c.*167del	NP_569082.2:n.*167del
XM_005273350.2:c.*167del	XP_005273407.1:n.*167del
XM_006711840.1:c.*167del	XP_006711903.1:n.*167del
XM_011544321.1:c.*167del	XP_011542623.1:n.*167del
XM_011544322.1:c.*167del	XP_011542624.1:n.*167del
XM_011544323.1:c.*167del	XP_011542625.1:n.*167del
XM_011544324.1:c.*167del	XP_011542626.1:n.*167del
XM_011544325.1:c.*167del	XP_011542627.1:n.*167del
XR_949162.1:n.2990+4260del
NM_001319224.1:c.*167del	NP_001306153.1:n.*167del
XM_006711840.2:c.*167del	XP_006711903.1:n.*167del
XM_011544321.2:c.*167del	XP_011542623.1:n.*167del
XM_011544323.2:c.*167del	XP_011542625.1:n.*167del
XM_011544324.2:c.*167del	XP_011542626.1:n.*167del
XM_011544325.2:c.*167del	XP_011542627.1:n.*167del
XM_017002793.2:c.*167del	XP_016858282.1:n.*167del
NM_130398.4:c.*167del MANE Select	NP_569082.2:n.*167del
NM_001319224.2:c.*167del	NP_001306153.1:n.*167del