Canonical Allele Identifier: CA1014053261

Gene: EXO1

Linked Data

• gnomAD v3: 1-241889774-C-CTTTTTTT
• gnomAD v4: 1-241889774-C-CTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241889779_241889780insTTTTTTT , CM000663.2:g.241889779_241889780insTTTTTTT	GRCh38
NC_000001.10:g.242053081_242053082insTTTTTTT , CM000663.1:g.242053081_242053082insTTTTTTT	GRCh37
NC_000001.9:g.240119704_240119705insTTTTTTT	NCBI36
NG_029100.1:g.46589_46590insTTTTTTT
NG_029100.2:g.46589_46590insTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.*179_*180insTTTTTTT MANE Select	ENSP00000355506.3:n.*179_*180insTTTTTTT
ENST00000348581.9:c.*179_*180insTTTTTTT	ENSP00000311873.5:n.*179_*180insTTTTTTT
ENST00000366548.7:c.*179_*180insTTTTTTT	ENSP00000355506.3:n.*179_*180insTTTTTTT
ENST00000518741.1:n.152-2745_152-2744insTTTTTTT
NM_003686.4:c.*306_*307insTTTTTTT	NP_003677.4:n.*306_*307insTTTTTTT
NM_006027.4:c.*179_*180insTTTTTTT	NP_006018.4:n.*179_*180insTTTTTTT
NM_130398.3:c.*179_*180insTTTTTTT	NP_569082.2:n.*179_*180insTTTTTTT
XM_005273350.2:c.*179_*180insTTTTTTT	XP_005273407.1:n.*179_*180insTTTTTTT
XM_006711840.1:c.*179_*180insTTTTTTT	XP_006711903.1:n.*179_*180insTTTTTTT
XM_011544321.1:c.*179_*180insTTTTTTT	XP_011542623.1:n.*179_*180insTTTTTTT
XM_011544322.1:c.*179_*180insTTTTTTT	XP_011542624.1:n.*179_*180insTTTTTTT
XM_011544323.1:c.*179_*180insTTTTTTT	XP_011542625.1:n.*179_*180insTTTTTTT
XM_011544324.1:c.*179_*180insTTTTTTT	XP_011542626.1:n.*179_*180insTTTTTTT
XM_011544325.1:c.*179_*180insTTTTTTT	XP_011542627.1:n.*179_*180insTTTTTTT
XR_949162.1:n.2990+4272_2990+4273insTTTTTTT
NM_001319224.1:c.*179_*180insTTTTTTT	NP_001306153.1:n.*179_*180insTTTTTTT
XM_006711840.2:c.*179_*180insTTTTTTT	XP_006711903.1:n.*179_*180insTTTTTTT
XM_011544321.2:c.*179_*180insTTTTTTT	XP_011542623.1:n.*179_*180insTTTTTTT
XM_011544323.2:c.*179_*180insTTTTTTT	XP_011542625.1:n.*179_*180insTTTTTTT
XM_011544324.2:c.*179_*180insTTTTTTT	XP_011542626.1:n.*179_*180insTTTTTTT
XM_011544325.2:c.*179_*180insTTTTTTT	XP_011542627.1:n.*179_*180insTTTTTTT
XM_017002793.2:c.*179_*180insTTTTTTT	XP_016858282.1:n.*179_*180insTTTTTTT
NM_130398.4:c.*179_*180insTTTTTTT MANE Select	NP_569082.2:n.*179_*180insTTTTTTT
NM_001319224.2:c.*179_*180insTTTTTTT	NP_001306153.1:n.*179_*180insTTTTTTT