Canonical Allele Identifier: CA1772946669

Gene: ESCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27780276A= , CM000670.2:g.27780276A=	GRCh38
NC_000008.10:g.27637793A= , CM000670.1:g.27637793A=	GRCh37
NC_000008.9:g.27693712A=	NCBI36
NG_008117.1:g.10736A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305188.13:c.955+9A= MANE Select	ENSP00000306999.8:n.955+9A=
ENST00000305188.12:c.955+9A=	ENSP00000306999.8:n.955+9A=
ENST00000518262.5:c.69+9A=
ENST00000522378.5:c.861+3107A=	ENSP00000428928.1:n.861+3107A=
NM_001017420.2:c.955+9A=	NP_001017420.1:n.955+9A=
XM_011544421.1:c.955+9A=	XP_011542723.1:n.955+9A=
XM_011544422.1:c.955+9A=	XP_011542724.1:n.955+9A=
XR_949378.1:n.1039+9A=
XR_949379.1:n.1039+9A=
XM_011544421.2:c.955+9A=	XP_011542723.1:n.955+9A=
XM_011544422.2:c.955+9A=	XP_011542724.1:n.955+9A=
XR_949378.3:n.1039+9A=
NM_001017420.3:c.955+9A= MANE Select	NP_001017420.1:n.955+9A=