Canonical Allele Identifier: CA1772950146

Gene: ESCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27787972A= , CM000670.2:g.27787972A=	GRCh38
NC_000008.10:g.27645489A= , CM000670.1:g.27645489A=	GRCh37
NC_000008.9:g.27701408A=	NCBI36
NG_008117.1:g.18432A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305188.13:c.1101A= MANE Select	ENSP00000306999.8:p.Thr367=
ENST00000305188.12:c.1101A=	ENSP00000306999.8:p.Thr367=
ENST00000397418.4:c.45A=	ENSP00000380563.2:p.Thr15=
ENST00000518262.5:c.215A=
ENST00000522378.5:c.*76A=	ENSP00000428928.1:n.*76A=
NM_001017420.2:c.1101A=	NP_001017420.1:p.Thr367=
XM_011544421.1:c.1101A=	XP_011542723.1:p.Thr367=
XM_011544422.1:c.1101A=	XP_011542724.1:p.Thr367=
XR_949378.1:n.1185A=
XR_949379.1:n.1185A=
XM_011544421.2:c.1101A=	XP_011542723.1:p.Thr367=
XM_011544422.2:c.1101A=	XP_011542724.1:p.Thr367=
XR_949378.3:n.1185A=
NM_001017420.3:c.1101A= MANE Select	NP_001017420.1:p.Thr367=