Canonical Allele Identifier: CA2748377848

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241889937del , CM000663.2:g.241889937del	GRCh38
NC_000001.10:g.242053239del , CM000663.1:g.242053239del	GRCh37
NC_000001.9:g.240119862del	NCBI36
NG_029100.1:g.46747del
NG_029100.2:g.46747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.*337del MANE Select	ENSP00000355506.3:n.*337del
ENST00000348581.9:c.*337del	ENSP00000311873.5:n.*337del
ENST00000366548.7:c.*337del	ENSP00000355506.3:n.*337del
ENST00000518741.1:n.152-2587del
NM_003686.4:c.*464del	NP_003677.4:n.*464del
NM_006027.4:c.*337del	NP_006018.4:n.*337del
NM_130398.3:c.*337del	NP_569082.2:n.*337del
XM_011544321.1:c.*337del	XP_011542623.1:n.*337del
XM_011544322.1:c.*337del	XP_011542624.1:n.*337del
XR_949162.1:n.2990+4430del
NM_001319224.1:c.*337del	NP_001306153.1:n.*337del
XM_006711840.2:c.*337del	XP_006711903.1:n.*337del
XM_011544321.2:c.*337del	XP_011542623.1:n.*337del
XM_011544323.2:c.*337del	XP_011542625.1:n.*337del
XM_011544324.2:c.*337del	XP_011542626.1:n.*337del
XM_011544325.2:c.*337del	XP_011542627.1:n.*337del
XM_017002793.2:c.*337del	XP_016858282.1:n.*337del
NM_130398.4:c.*337del MANE Select	NP_569082.2:n.*337del
NM_001319224.2:c.*337del	NP_001306153.1:n.*337del