Canonical Allele Identifier: CA1480985
Gene: EXO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241853415G>A , CM000663.2:g.241853415G>A GRCh38
NC_000001.10:g.242016717G>A , CM000663.1:g.242016717G>A GRCh37
NC_000001.9:g.240083340G>A NCBI36
NG_029100.1:g.10225G>A
NG_029100.2:g.10225G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366548.8:c.339G>A MANE Select ENSP00000355506.3:p.Ser113=
ENST00000348581.9:c.339G>A ENSP00000311873.5:p.Ser113=
ENST00000366548.7:c.339G>A ENSP00000355506.3:p.Ser113=
ENST00000423131.5:c.219G>A ENSP00000415531.1:p.Ser73=
ENST00000437497.5:c.219G>A ENSP00000412041.1:p.Ser73=
ENST00000450748.1:c.339G>A ENSP00000406652.1:p.Ser113=
ENST00000469419.1:n.215+1004G>A
ENST00000493702.5:n.281G>A
ENST00000518483.5:c.339G>A ENSP00000430251.1:p.Ser113=
ENST00000523590.5:c.219G>A ENSP00000430082.1:p.Ser73=
NM_003686.4:c.339G>A NP_003677.4:p.Ser113=
NM_006027.4:c.339G>A NP_006018.4:p.Ser113=
NM_130398.3:c.339G>A NP_569082.2:p.Ser113=
XM_005273350.2:c.339G>A XP_005273407.1:p.Ser113=
XM_006711840.1:c.339G>A XP_006711903.1:p.Ser113=
XM_011544321.1:c.339G>A XP_011542623.1:p.Ser113=
XM_011544322.1:c.339G>A XP_011542624.1:p.Ser113=
XM_011544323.1:c.339G>A XP_011542625.1:p.Ser113=
XM_011544324.1:c.219G>A XP_011542626.1:p.Ser73=
XM_011544326.1:c.339G>A XP_011542628.1:p.Ser113=
XM_011544327.1:c.339G>A XP_011542629.1:p.Ser113=
XR_949162.1:n.924G>A
NM_001319224.1:c.339G>A NP_001306153.1:p.Ser113=
XM_006711840.2:c.339G>A XP_006711903.1:p.Ser113=
XM_011544321.2:c.339G>A XP_011542623.1:p.Ser113=
XM_011544323.2:c.339G>A XP_011542625.1:p.Ser113=
XM_011544324.2:c.219G>A XP_011542626.1:p.Ser73=
XM_017002793.2:c.219G>A XP_016858282.1:p.Ser73=
NM_130398.4:c.339G>A MANE Select NP_569082.2:p.Ser113=
NM_001319224.2:c.339G>A NP_001306153.1:p.Ser113=