Canonical Allele Identifier: CA1772950148
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27787974G= , CM000670.2:g.27787974G= GRCh38
NC_000008.10:g.27645491G= , CM000670.1:g.27645491G= GRCh37
NC_000008.9:g.27701410G= NCBI36
NG_008117.1:g.18434G=

Transcript Alleles

HGVS Amino-acid change
ENST00000305188.13:c.1103G= MANE Select ENSP00000306999.8:p.Ser368=
ENST00000305188.12:c.1103G= ENSP00000306999.8:p.Ser368=
ENST00000397418.4:c.47G= ENSP00000380563.2:p.Ser16=
ENST00000518262.5:c.217G=
ENST00000522378.5:c.*78G= ENSP00000428928.1:n.*78G=
NM_001017420.2:c.1103G= NP_001017420.1:p.Ser368=
XM_011544421.1:c.1103G= XP_011542723.1:p.Ser368=
XM_011544422.1:c.1103G= XP_011542724.1:p.Ser368=
XR_949378.1:n.1187G=
XR_949379.1:n.1187G=
XM_011544421.2:c.1103G= XP_011542723.1:p.Ser368=
XM_011544422.2:c.1103G= XP_011542724.1:p.Ser368=
XR_949378.3:n.1187G=
NM_001017420.3:c.1103G= MANE Select NP_001017420.1:p.Ser368=