Canonical Allele Identifier: CA345462367
Gene: EXO1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241889569G>T , CM000663.2:g.241889569G>T GRCh38
NC_000001.10:g.242052871G>T , CM000663.1:g.242052871G>T GRCh37
NC_000001.9:g.240119494G>T NCBI36
NG_029100.1:g.46379G>T
NG_029100.2:g.46379G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366548.8:c.2510G>T MANE Select ENSP00000355506.3:p.Cys837Phe
ENST00000348581.9:c.2510G>T ENSP00000311873.5:p.Cys837Phe
ENST00000366548.7:c.2510G>T ENSP00000355506.3:p.Cys837Phe
ENST00000518483.5:c.*96G>T ENSP00000430251.1:n.*96G>T
ENST00000518741.1:n.152-2955G>T
ENST00000521202.2:c.603G>T
NM_003686.4:c.*96G>T NP_003677.4:n.*96G>T
NM_006027.4:c.2510G>T NP_006018.4:p.Cys837Phe
NM_130398.3:c.2510G>T NP_569082.2:p.Cys837Phe
XM_005273350.2:c.2507G>T XP_005273407.1:p.Cys836Phe
XM_006711840.1:c.2510G>T XP_006711903.1:p.Cys837Phe
XM_011544321.1:c.2510G>T XP_011542623.1:p.Cys837Phe
XM_011544322.1:c.2510G>T XP_011542624.1:p.Cys837Phe
XM_011544323.1:c.2507G>T XP_011542625.1:p.Cys836Phe
XM_011544324.1:c.2390G>T XP_011542626.1:p.Cys797Phe
XM_011544325.1:c.1547G>T XP_011542627.1:p.Cys516Phe
XR_949162.1:n.2990+4062G>T
NM_001319224.1:c.2507G>T NP_001306153.1:p.Cys836Phe
XM_006711840.2:c.2510G>T XP_006711903.1:p.Cys837Phe
XM_011544321.2:c.2510G>T XP_011542623.1:p.Cys837Phe
XM_011544323.2:c.2507G>T XP_011542625.1:p.Cys836Phe
XM_011544324.2:c.2390G>T XP_011542626.1:p.Cys797Phe
XM_011544325.2:c.1547G>T XP_011542627.1:p.Cys516Phe
XM_017002793.2:c.2390G>T XP_016858282.1:p.Cys797Phe
NM_130398.4:c.2510G>T MANE Select NP_569082.2:p.Cys837Phe
NM_001319224.2:c.2507G>T NP_001306153.1:p.Cys836Phe