Canonical Allele Identifier: CA1229737389

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241889863C= , CM000663.2:g.241889863C=	GRCh38
NC_000001.10:g.242053165C= , CM000663.1:g.242053165C=	GRCh37
NC_000001.9:g.240119788C=	NCBI36
NG_029100.1:g.46673C=
NG_029100.2:g.46673C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366548.8:c.*263C= MANE Select	ENSP00000355506.3:n.*263C=
ENST00000348581.9:c.*263C=	ENSP00000311873.5:n.*263C=
ENST00000366548.7:c.*263C=	ENSP00000355506.3:n.*263C=
ENST00000518741.1:n.152-2661C=
NM_003686.4:c.*390C=	NP_003677.4:n.*390C=
NM_006027.4:c.*263C=	NP_006018.4:n.*263C=
NM_130398.3:c.*263C=	NP_569082.2:n.*263C=
XM_011544321.1:c.*263C=	XP_011542623.1:n.*263C=
XM_011544322.1:c.*263C=	XP_011542624.1:n.*263C=
XR_949162.1:n.2990+4356C=
NM_001319224.1:c.*263C=	NP_001306153.1:n.*263C=
XM_006711840.2:c.*263C=	XP_006711903.1:n.*263C=
XM_011544321.2:c.*263C=	XP_011542623.1:n.*263C=
XM_011544323.2:c.*263C=	XP_011542625.1:n.*263C=
XM_011544324.2:c.*263C=	XP_011542626.1:n.*263C=
XM_011544325.2:c.*263C=	XP_011542627.1:n.*263C=
XM_017002793.2:c.*263C=	XP_016858282.1:n.*263C=
NM_130398.4:c.*263C= MANE Select	NP_569082.2:n.*263C=
NM_001319224.2:c.*263C=	NP_001306153.1:n.*263C=