Canonical Allele Identifier: CA2544704047

Gene: EXO1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241877415C>A , CM000663.2:g.241877415C>A	GRCh38
NC_000001.10:g.242040717C>A , CM000663.1:g.242040717C>A	GRCh37
NC_000001.9:g.240107340C>A	NCBI36
NG_029100.1:g.34225C>A
NG_029100.2:g.34225C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366548.8:c.1515-1334C>A MANE Select	ENSP00000355506.3:n.1515-1334C>A
ENST00000348581.9:c.1515-1334C>A	ENSP00000311873.5:n.1515-1334C>A
ENST00000366548.7:c.1515-1334C>A	ENSP00000355506.3:n.1515-1334C>A
ENST00000518483.5:c.1515-1334C>A	ENSP00000430251.1:n.1515-1334C>A
NM_003686.4:c.1515-1334C>A	NP_003677.4:n.1515-1334C>A
NM_006027.4:c.1515-1334C>A	NP_006018.4:n.1515-1334C>A
NM_130398.3:c.1515-1334C>A	NP_569082.2:n.1515-1334C>A
XM_005273350.2:c.1512-1334C>A	XP_005273407.1:n.1512-1334C>A
XM_006711840.1:c.1515-1334C>A	XP_006711903.1:n.1515-1334C>A
XM_011544321.1:c.1515-1334C>A	XP_011542623.1:n.1515-1334C>A
XM_011544322.1:c.1515-1334C>A	XP_011542624.1:n.1515-1334C>A
XM_011544323.1:c.1512-1334C>A	XP_011542625.1:n.1512-1334C>A
XM_011544324.1:c.1395-1334C>A	XP_011542626.1:n.1395-1334C>A
XM_011544325.1:c.552-1334C>A	XP_011542627.1:n.552-1334C>A
XM_011544326.1:c.1517-1335C>A	XP_011542628.1:n.1517-1335C>A
XR_949162.1:n.2100-1334C>A
NM_001319224.1:c.1512-1334C>A	NP_001306153.1:n.1512-1334C>A
XM_006711840.2:c.1515-1334C>A	XP_006711903.1:n.1515-1334C>A
XM_011544321.2:c.1515-1334C>A	XP_011542623.1:n.1515-1334C>A
XM_011544323.2:c.1512-1334C>A	XP_011542625.1:n.1512-1334C>A
XM_011544324.2:c.1395-1334C>A	XP_011542626.1:n.1395-1334C>A
XM_011544325.2:c.552-1334C>A	XP_011542627.1:n.552-1334C>A
XM_017002793.2:c.1395-1334C>A	XP_016858282.1:n.1395-1334C>A
NM_130398.4:c.1515-1334C>A MANE Select	NP_569082.2:n.1515-1334C>A
NM_001319224.2:c.1512-1334C>A	NP_001306153.1:n.1512-1334C>A