Canonical Allele Identifier: CA1772950145
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27787971C= , CM000670.2:g.27787971C= GRCh38
NC_000008.10:g.27645488C= , CM000670.1:g.27645488C= GRCh37
NC_000008.9:g.27701407C= NCBI36
NG_008117.1:g.18431C=

Transcript Alleles

HGVS Amino-acid change
ENST00000305188.13:c.1100C= MANE Select ENSP00000306999.8:p.Thr367=
ENST00000305188.12:c.1100C= ENSP00000306999.8:p.Thr367=
ENST00000397418.4:c.44C= ENSP00000380563.2:p.Thr15=
ENST00000518262.5:c.214C=
ENST00000522378.5:c.*75C= ENSP00000428928.1:n.*75C=
NM_001017420.2:c.1100C= NP_001017420.1:p.Thr367=
XM_011544421.1:c.1100C= XP_011542723.1:p.Thr367=
XM_011544422.1:c.1100C= XP_011542724.1:p.Thr367=
XR_949378.1:n.1184C=
XR_949379.1:n.1184C=
XM_011544421.2:c.1100C= XP_011542723.1:p.Thr367=
XM_011544422.2:c.1100C= XP_011542724.1:p.Thr367=
XR_949378.3:n.1184C=
NM_001017420.3:c.1100C= MANE Select NP_001017420.1:p.Thr367=