Canonical Allele Identifier: CA1229734161

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241881982C= , CM000663.2:g.241881982C=	GRCh38
NC_000001.10:g.242045284C= , CM000663.1:g.242045284C=	GRCh37
NC_000001.9:g.240111907C=	NCBI36
NG_029100.1:g.38792C=
NG_029100.2:g.38792C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366548.8:c.2176C= MANE Select	ENSP00000355506.3:p.His726=
ENST00000348581.9:c.2176C=	ENSP00000311873.5:p.His726=
ENST00000366548.7:c.2176C=	ENSP00000355506.3:p.His726=
ENST00000518483.5:c.2176C=	ENSP00000430251.1:p.His726=
ENST00000521202.2:c.304+2639C=
NM_003686.4:c.2176C=	NP_003677.4:p.His726=
NM_006027.4:c.2176C=	NP_006018.4:p.His726=
NM_130398.3:c.2176C=	NP_569082.2:p.His726=
XM_005273350.2:c.2173C=	XP_005273407.1:p.His725=
XM_006711840.1:c.2176C=	XP_006711903.1:p.His726=
XM_011544321.1:c.2176C=	XP_011542623.1:p.His726=
XM_011544322.1:c.2176C=	XP_011542624.1:p.His726=
XM_011544323.1:c.2173C=	XP_011542625.1:p.His725=
XM_011544324.1:c.2056C=	XP_011542626.1:p.His686=
XM_011544325.1:c.1213C=	XP_011542627.1:p.His405=
XR_949162.1:n.2761C=
NM_001319224.1:c.2173C=	NP_001306153.1:p.His725=
XM_006711840.2:c.2176C=	XP_006711903.1:p.His726=
XM_011544321.2:c.2176C=	XP_011542623.1:p.His726=
XM_011544323.2:c.2173C=	XP_011542625.1:p.His725=
XM_011544324.2:c.2056C=	XP_011542626.1:p.His686=
XM_011544325.2:c.1213C=	XP_011542627.1:p.His405=
XM_017002793.2:c.2056C=	XP_016858282.1:p.His686=
NM_130398.4:c.2176C= MANE Select	NP_569082.2:p.His726=
NM_001319224.2:c.2173C=	NP_001306153.1:p.His725=