Canonical Allele Identifier: CA1772950162

Gene: ESCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27788003G= , CM000670.2:g.27788003G=	GRCh38
NC_000008.10:g.27645520G= , CM000670.1:g.27645520G=	GRCh37
NC_000008.9:g.27701439G=	NCBI36
NG_008117.1:g.18463G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305188.13:c.1131+1G= MANE Select	ENSP00000306999.8:n.1131+1G=
ENST00000305188.12:c.1131+1G=	ENSP00000306999.8:n.1131+1G=
ENST00000397418.4:c.75+1G=	ENSP00000380563.2:n.75+1G=
ENST00000518262.5:c.245+1G=
ENST00000522378.5:c.*106+1G=	ENSP00000428928.1:n.*106+1G=
NM_001017420.2:c.1131+1G=	NP_001017420.1:n.1131+1G=
XM_011544421.1:c.1131+1G=	XP_011542723.1:n.1131+1G=
XM_011544422.1:c.1131+1G=	XP_011542724.1:n.1131+1G=
XR_949378.1:n.1215+1G=
XR_949379.1:n.1215+1G=
XM_011544421.2:c.1131+1G=	XP_011542723.1:n.1131+1G=
XM_011544422.2:c.1131+1G=	XP_011542724.1:n.1131+1G=
XR_949378.3:n.1215+1G=
NM_001017420.3:c.1131+1G= MANE Select	NP_001017420.1:n.1131+1G=