Canonical Allele Identifier: CA1772950150

Gene: ESCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27787976A= , CM000670.2:g.27787976A=	GRCh38
NC_000008.10:g.27645493A= , CM000670.1:g.27645493A=	GRCh37
NC_000008.9:g.27701412A=	NCBI36
NG_008117.1:g.18436A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305188.13:c.1105A= MANE Select	ENSP00000306999.8:p.Lys369=
ENST00000305188.12:c.1105A=	ENSP00000306999.8:p.Lys369=
ENST00000397418.4:c.49A=	ENSP00000380563.2:p.Lys17=
ENST00000518262.5:c.219A=
ENST00000522378.5:c.*80A=	ENSP00000428928.1:n.*80A=
NM_001017420.2:c.1105A=	NP_001017420.1:p.Lys369=
XM_011544421.1:c.1105A=	XP_011542723.1:p.Lys369=
XM_011544422.1:c.1105A=	XP_011542724.1:p.Lys369=
XR_949378.1:n.1189A=
XR_949379.1:n.1189A=
XM_011544421.2:c.1105A=	XP_011542723.1:p.Lys369=
XM_011544422.2:c.1105A=	XP_011542724.1:p.Lys369=
XR_949378.3:n.1189A=
NM_001017420.3:c.1105A= MANE Select	NP_001017420.1:p.Lys369=