Canonical Allele Identifier: CA2651276753

Gene: EXO1

Linked Data

• gnomAD v4: 1-241889866-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241889866G>A , CM000663.2:g.241889866G>A	GRCh38
NC_000001.10:g.242053168G>A , CM000663.1:g.242053168G>A	GRCh37
NC_000001.9:g.240119791G>A	NCBI36
NG_029100.1:g.46676G>A
NG_029100.2:g.46676G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.*266G>A MANE Select	ENSP00000355506.3:n.*266G>A
ENST00000348581.9:c.*266G>A	ENSP00000311873.5:n.*266G>A
ENST00000366548.7:c.*266G>A	ENSP00000355506.3:n.*266G>A
ENST00000518741.1:n.152-2658G>A
NM_003686.4:c.*393G>A	NP_003677.4:n.*393G>A
NM_006027.4:c.*266G>A	NP_006018.4:n.*266G>A
NM_130398.3:c.*266G>A	NP_569082.2:n.*266G>A
XM_011544321.1:c.*266G>A	XP_011542623.1:n.*266G>A
XM_011544322.1:c.*266G>A	XP_011542624.1:n.*266G>A
XR_949162.1:n.2990+4359G>A
NM_001319224.1:c.*266G>A	NP_001306153.1:n.*266G>A
XM_006711840.2:c.*266G>A	XP_006711903.1:n.*266G>A
XM_011544321.2:c.*266G>A	XP_011542623.1:n.*266G>A
XM_011544323.2:c.*266G>A	XP_011542625.1:n.*266G>A
XM_011544324.2:c.*266G>A	XP_011542626.1:n.*266G>A
XM_011544325.2:c.*266G>A	XP_011542627.1:n.*266G>A
XM_017002793.2:c.*266G>A	XP_016858282.1:n.*266G>A
NM_130398.4:c.*266G>A MANE Select	NP_569082.2:n.*266G>A
NM_001319224.2:c.*266G>A	NP_001306153.1:n.*266G>A