Canonical Allele Identifier: CA1139885484

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241848731G= , CM000663.2:g.241848731G=	GRCh38
NC_000001.10:g.242012033G= , CM000663.1:g.242012033G=	GRCh37
NC_000001.9:g.240078656G=	NCBI36
NG_029100.1:g.5541G=
NG_029100.2:g.5541G=

Transcript Alleles

HGVS	Amino-acid Change
NM_130398.4:c.-419G= MANE Select	NP_569082.2:n.-419G=
ENST00000366548.8:c.-419G= MANE Select	ENSP00000355506.3:n.-419G=
NM_001319224.1:c.-314G=	NP_001306153.1:n.-314G=
NM_001319224.2:c.-314G=	NP_001306153.1:n.-314G=
NM_003686.4:c.-314G=	NP_003677.4:n.-314G=
NM_006027.4:c.-314G=	NP_006018.4:n.-314G=
NM_130398.3:c.-419G=	NP_569082.2:n.-419G=
ENST00000348581.9:c.-314G=	ENSP00000311873.5:n.-314G=
ENST00000366548.7:c.-419G=	ENSP00000355506.3:n.-419G=
ENST00000423131.5:c.-314G=	ENSP00000415531.1:n.-314G=
ENST00000519225.5:c.-314G=	ENSP00000429720.1:n.-314G=
ENST00000523590.5:c.-314G=	ENSP00000430082.1:n.-314G=
XM_005273350.2:c.-314G=	XP_005273407.1:n.-314G=
XM_006711840.1:c.-422G=	XP_006711903.1:n.-422G=
XM_006711840.2:c.-422G=	XP_006711903.1:n.-422G=
XM_011544321.1:c.-314G=	XP_011542623.1:n.-314G=
XM_011544321.2:c.-314G=	XP_011542623.1:n.-314G=
XM_011544322.1:c.-314G=	XP_011542624.1:n.-314G=
XM_011544323.1:c.-422G=	XP_011542625.1:n.-422G=
XM_011544323.2:c.-422G=	XP_011542625.1:n.-422G=
XM_011544324.1:c.-422G=	XP_011542626.1:n.-422G=
XM_011544324.2:c.-422G=	XP_011542626.1:n.-422G=
XM_011544326.1:c.-422G=	XP_011542628.1:n.-422G=
XM_011544327.1:c.-422G=	XP_011542629.1:n.-422G=
XM_017002793.2:c.-314G=	XP_016858282.1:n.-314G=
XR_949162.1:n.164G=