Canonical Allele Identifier: CA1014053290

Gene: EXO1

Linked Data

• dbSNP Id: rs1663284482
• gnomAD v3: 1-241889938-A-T
• gnomAD v4: 1-241889938-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241889938A>T , CM000663.2:g.241889938A>T	GRCh38
NC_000001.10:g.242053240A>T , CM000663.1:g.242053240A>T	GRCh37
NC_000001.9:g.240119863A>T	NCBI36
NG_029100.1:g.46748A>T
NG_029100.2:g.46748A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.*338A>T MANE Select	ENSP00000355506.3:n.*338A>T
ENST00000366548.7:c.*338A>T	ENSP00000355506.3:n.*338A>T
ENST00000518741.1:n.152-2586A>T
NM_003686.4:c.*465A>T	NP_003677.4:n.*465A>T
NM_006027.4:c.*338A>T	NP_006018.4:n.*338A>T
NM_130398.3:c.*338A>T	NP_569082.2:n.*338A>T
XM_011544321.1:c.*338A>T	XP_011542623.1:n.*338A>T
XM_011544322.1:c.*338A>T	XP_011542624.1:n.*338A>T
XR_949162.1:n.2990+4431A>T
NM_001319224.1:c.*338A>T	NP_001306153.1:n.*338A>T
XM_006711840.2:c.*338A>T	XP_006711903.1:n.*338A>T
XM_011544321.2:c.*338A>T	XP_011542623.1:n.*338A>T
XM_011544323.2:c.*338A>T	XP_011542625.1:n.*338A>T
XM_011544324.2:c.*338A>T	XP_011542626.1:n.*338A>T
XM_011544325.2:c.*338A>T	XP_011542627.1:n.*338A>T
XM_017002793.2:c.*338A>T	XP_016858282.1:n.*338A>T
NM_130398.4:c.*338A>T MANE Select	NP_569082.2:n.*338A>T
NM_001319224.2:c.*338A>T	NP_001306153.1:n.*338A>T