Canonical Allele Identifier: CA1480897

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241850524C>T , CM000663.2:g.241850524C>T	GRCh38
NC_000001.10:g.242013826C>T , CM000663.1:g.242013826C>T	GRCh37
NC_000001.9:g.240080449C>T	NCBI36
NG_029100.1:g.7334C>T
NG_029100.2:g.7334C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.99C>T MANE Select	ENSP00000355506.3:p.Cys33=
ENST00000348581.9:c.99C>T	ENSP00000311873.5:p.Cys33=
ENST00000366548.7:c.99C>T	ENSP00000355506.3:p.Cys33=
ENST00000423131.5:c.99C>T	ENSP00000415531.1:p.Cys33=
ENST00000437497.5:c.99C>T	ENSP00000412041.1:p.Cys33=
ENST00000450748.1:c.99C>T	ENSP00000406652.1:p.Cys33=
ENST00000469419.1:n.33C>T
ENST00000493702.5:n.161C>T
ENST00000518483.5:c.99C>T	ENSP00000430251.1:p.Cys33=
ENST00000523590.5:c.99C>T	ENSP00000430082.1:p.Cys33=
NM_003686.4:c.99C>T	NP_003677.4:p.Cys33=
NM_006027.4:c.99C>T	NP_006018.4:p.Cys33=
NM_130398.3:c.99C>T	NP_569082.2:p.Cys33=
XM_005273350.2:c.99C>T	XP_005273407.1:p.Cys33=
XM_006711840.1:c.99C>T	XP_006711903.1:p.Cys33=
XM_011544321.1:c.99C>T	XP_011542623.1:p.Cys33=
XM_011544322.1:c.99C>T	XP_011542624.1:p.Cys33=
XM_011544323.1:c.99C>T	XP_011542625.1:p.Cys33=
XM_011544324.1:c.99C>T	XP_011542626.1:p.Cys33=
XM_011544326.1:c.99C>T	XP_011542628.1:p.Cys33=
XM_011544327.1:c.99C>T	XP_011542629.1:p.Cys33=
XR_949162.1:n.684C>T
NM_001319224.1:c.99C>T	NP_001306153.1:p.Cys33=
XM_006711840.2:c.99C>T	XP_006711903.1:p.Cys33=
XM_011544321.2:c.99C>T	XP_011542623.1:p.Cys33=
XM_011544323.2:c.99C>T	XP_011542625.1:p.Cys33=
XM_011544324.2:c.99C>T	XP_011542626.1:p.Cys33=
XM_017002793.2:c.99C>T	XP_016858282.1:p.Cys33=
NM_130398.4:c.99C>T MANE Select	NP_569082.2:p.Cys33=
NM_001319224.2:c.99C>T	NP_001306153.1:p.Cys33=