Canonical Allele Identifier: CA345451360

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241860580G>C , CM000663.2:g.241860580G>C	GRCh38
NC_000001.10:g.242023882G>C , CM000663.1:g.242023882G>C	GRCh37
NC_000001.9:g.240090505G>C	NCBI36
NG_029100.1:g.17390G>C
NG_029100.2:g.17390G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.820G>C MANE Select	ENSP00000355506.3:p.Gly274Arg
ENST00000348581.9:c.820G>C	ENSP00000311873.5:p.Gly274Arg
ENST00000366548.7:c.820G>C	ENSP00000355506.3:p.Gly274Arg
ENST00000469419.1:n.630G>C
ENST00000518483.5:c.820G>C	ENSP00000430251.1:p.Gly274Arg
NM_003686.4:c.820G>C	NP_003677.4:p.Gly274Arg
NM_006027.4:c.820G>C	NP_006018.4:p.Gly274Arg
NM_130398.3:c.820G>C	NP_569082.2:p.Gly274Arg
XM_005273350.2:c.820G>C	XP_005273407.1:p.Gly274Arg
XM_006711840.1:c.820G>C	XP_006711903.1:p.Gly274Arg
XM_011544321.1:c.820G>C	XP_011542623.1:p.Gly274Arg
XM_011544322.1:c.820G>C	XP_011542624.1:p.Gly274Arg
XM_011544323.1:c.820G>C	XP_011542625.1:p.Gly274Arg
XM_011544324.1:c.700G>C	XP_011542626.1:p.Gly234Arg
XM_011544326.1:c.820G>C	XP_011542628.1:p.Gly274Arg
XM_011544327.1:c.820G>C	XP_011542629.1:p.Gly274Arg
XR_949162.1:n.1405G>C
NM_001319224.1:c.820G>C	NP_001306153.1:p.Gly274Arg
XM_006711840.2:c.820G>C	XP_006711903.1:p.Gly274Arg
XM_011544321.2:c.820G>C	XP_011542623.1:p.Gly274Arg
XM_011544323.2:c.820G>C	XP_011542625.1:p.Gly274Arg
XM_011544324.2:c.700G>C	XP_011542626.1:p.Gly234Arg
XM_017002793.2:c.700G>C	XP_016858282.1:p.Gly234Arg
NM_130398.4:c.820G>C MANE Select	NP_569082.2:p.Gly274Arg
NM_001319224.2:c.820G>C	NP_001306153.1:p.Gly274Arg