Canonical Allele Identifier: CA1772944965

Gene: ESCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27776813C= , CM000670.2:g.27776813C=	GRCh38
NC_000008.10:g.27634330C= , CM000670.1:g.27634330C=	GRCh37
NC_000008.9:g.27690249C=	NCBI36
NG_008117.1:g.7273C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305188.13:c.505C= MANE Select	ENSP00000306999.8:p.Arg169=
ENST00000305188.12:c.505C=	ENSP00000306999.8:p.Arg169=
ENST00000522378.5:c.505C=	ENSP00000428928.1:p.Arg169=
ENST00000523566.5:c.505C=	ENSP00000428435.1:p.Arg169=
ENST00000523910.1:n.304C=
ENST00000524293.1:n.523C=
NM_001017420.2:c.505C=	NP_001017420.1:p.Arg169=
XM_011544421.1:c.505C=	XP_011542723.1:p.Arg169=
XM_011544422.1:c.505C=	XP_011542724.1:p.Arg169=
XR_949378.1:n.589C=
XR_949379.1:n.589C=
XM_011544421.2:c.505C=	XP_011542723.1:p.Arg169=
XM_011544422.2:c.505C=	XP_011542724.1:p.Arg169=
XR_949378.3:n.589C=
NM_001017420.3:c.505C= MANE Select	NP_001017420.1:p.Arg169=