Canonical Allele Identifier: CA1772993439

Gene: ESCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27799658T= , CM000670.2:g.27799658T=	GRCh38
NC_000008.10:g.27657175T= , CM000670.1:g.27657175T=	GRCh37
NC_000008.9:g.27713094T=	NCBI36
NG_008117.1:g.30118T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305188.13:c.1615T= MANE Select	ENSP00000306999.8:p.Trp539=
ENST00000305188.12:c.1615T=	ENSP00000306999.8:p.Trp539=
ENST00000397418.4:c.559T=	ENSP00000380563.2:p.Trp187=
ENST00000522378.5:c.*590T=	ENSP00000428928.1:n.*590T=
NM_001017420.2:c.1615T=	NP_001017420.1:p.Trp539=
XM_011544421.1:c.1615T=	XP_011542723.1:p.Trp539=
XM_011544422.1:c.1615T=	XP_011542724.1:p.Trp539=
XR_949378.1:n.1699T=
XR_949379.1:n.1699T=
XM_011544421.2:c.1615T=	XP_011542723.1:p.Trp539=
XM_011544422.2:c.1615T=	XP_011542724.1:p.Trp539=
XR_949378.3:n.1699T=
NM_001017420.3:c.1615T= MANE Select	NP_001017420.1:p.Trp539=