Canonical Allele Identifier: CA2651276658

Gene: EXO1

Linked Data

• gnomAD v4: 1-241889741-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241889741A>C , CM000663.2:g.241889741A>C	GRCh38
NC_000001.10:g.242053043A>C , CM000663.1:g.242053043A>C	GRCh37
NC_000001.9:g.240119666A>C	NCBI36
NG_029100.1:g.46551A>C
NG_029100.2:g.46551A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.*141A>C MANE Select	ENSP00000355506.3:n.*141A>C
ENST00000348581.9:c.*141A>C	ENSP00000311873.5:n.*141A>C
ENST00000366548.7:c.*141A>C	ENSP00000355506.3:n.*141A>C
ENST00000518483.5:c.*268A>C	ENSP00000430251.1:n.*268A>C
ENST00000518741.1:n.152-2783A>C
NM_003686.4:c.*268A>C	NP_003677.4:n.*268A>C
NM_006027.4:c.*141A>C	NP_006018.4:n.*141A>C
NM_130398.3:c.*141A>C	NP_569082.2:n.*141A>C
XM_005273350.2:c.*141A>C	XP_005273407.1:n.*141A>C
XM_006711840.1:c.*141A>C	XP_006711903.1:n.*141A>C
XM_011544321.1:c.*141A>C	XP_011542623.1:n.*141A>C
XM_011544322.1:c.*141A>C	XP_011542624.1:n.*141A>C
XM_011544323.1:c.*141A>C	XP_011542625.1:n.*141A>C
XM_011544324.1:c.*141A>C	XP_011542626.1:n.*141A>C
XM_011544325.1:c.*141A>C	XP_011542627.1:n.*141A>C
XR_949162.1:n.2990+4234A>C
NM_001319224.1:c.*141A>C	NP_001306153.1:n.*141A>C
XM_006711840.2:c.*141A>C	XP_006711903.1:n.*141A>C
XM_011544321.2:c.*141A>C	XP_011542623.1:n.*141A>C
XM_011544323.2:c.*141A>C	XP_011542625.1:n.*141A>C
XM_011544324.2:c.*141A>C	XP_011542626.1:n.*141A>C
XM_011544325.2:c.*141A>C	XP_011542627.1:n.*141A>C
XM_017002793.2:c.*141A>C	XP_016858282.1:n.*141A>C
NM_130398.4:c.*141A>C MANE Select	NP_569082.2:n.*141A>C
NM_001319224.2:c.*141A>C	NP_001306153.1:n.*141A>C