Canonical Allele Identifier: CA1772950147
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27787973A= , CM000670.2:g.27787973A= GRCh38
NC_000008.10:g.27645490A= , CM000670.1:g.27645490A= GRCh37
NC_000008.9:g.27701409A= NCBI36
NG_008117.1:g.18433A=

Transcript Alleles

HGVS Amino-acid change
ENST00000305188.13:c.1102A= MANE Select ENSP00000306999.8:p.Ser368=
ENST00000305188.12:c.1102A= ENSP00000306999.8:p.Ser368=
ENST00000397418.4:c.46A= ENSP00000380563.2:p.Ser16=
ENST00000518262.5:c.216A=
ENST00000522378.5:c.*77A= ENSP00000428928.1:n.*77A=
NM_001017420.2:c.1102A= NP_001017420.1:p.Ser368=
XM_011544421.1:c.1102A= XP_011542723.1:p.Ser368=
XM_011544422.1:c.1102A= XP_011542724.1:p.Ser368=
XR_949378.1:n.1186A=
XR_949379.1:n.1186A=
XM_011544421.2:c.1102A= XP_011542723.1:p.Ser368=
XM_011544422.2:c.1102A= XP_011542724.1:p.Ser368=
XR_949378.3:n.1186A=
NM_001017420.3:c.1102A= MANE Select NP_001017420.1:p.Ser368=