Canonical Allele Identifier: CA345462355

Gene: EXO1

Linked Data

• dbSNP Id: rs1663265879
• gnomAD v3: 1-241889565-G-C
• gnomAD v4: 1-241889565-G-C
• MyVariant Identifiers: chr1:g.242052867G>C (hg19) ; chr1:g.241889565G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241889565G>C , CM000663.2:g.241889565G>C	GRCh38
NC_000001.10:g.242052867G>C , CM000663.1:g.242052867G>C	GRCh37
NC_000001.9:g.240119490G>C	NCBI36
NG_029100.1:g.46375G>C
NG_029100.2:g.46375G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.2506G>C MANE Select	ENSP00000355506.3:p.Glu836Gln
ENST00000348581.9:c.2506G>C	ENSP00000311873.5:p.Glu836Gln
ENST00000366548.7:c.2506G>C	ENSP00000355506.3:p.Glu836Gln
ENST00000518483.5:c.*92G>C	ENSP00000430251.1:n.*92G>C
ENST00000518741.1:n.152-2959G>C
ENST00000521202.2:c.599G>C
NM_003686.4:c.*92G>C	NP_003677.4:n.*92G>C
NM_006027.4:c.2506G>C	NP_006018.4:p.Glu836Gln
NM_130398.3:c.2506G>C	NP_569082.2:p.Glu836Gln
XM_005273350.2:c.2503G>C	XP_005273407.1:p.Glu835Gln
XM_006711840.1:c.2506G>C	XP_006711903.1:p.Glu836Gln
XM_011544321.1:c.2506G>C	XP_011542623.1:p.Glu836Gln
XM_011544322.1:c.2506G>C	XP_011542624.1:p.Glu836Gln
XM_011544323.1:c.2503G>C	XP_011542625.1:p.Glu835Gln
XM_011544324.1:c.2386G>C	XP_011542626.1:p.Glu796Gln
XM_011544325.1:c.1543G>C	XP_011542627.1:p.Glu515Gln
XR_949162.1:n.2990+4058G>C
NM_001319224.1:c.2503G>C	NP_001306153.1:p.Glu835Gln
XM_006711840.2:c.2506G>C	XP_006711903.1:p.Glu836Gln
XM_011544321.2:c.2506G>C	XP_011542623.1:p.Glu836Gln
XM_011544323.2:c.2503G>C	XP_011542625.1:p.Glu835Gln
XM_011544324.2:c.2386G>C	XP_011542626.1:p.Glu796Gln
XM_011544325.2:c.1543G>C	XP_011542627.1:p.Glu515Gln
XM_017002793.2:c.2386G>C	XP_016858282.1:p.Glu796Gln
NM_130398.4:c.2506G>C MANE Select	NP_569082.2:p.Glu836Gln
NM_001319224.2:c.2503G>C	NP_001306153.1:p.Glu835Gln