Canonical Allele Identifier: CA271498
Community Standard Title: NM_001017420.3(ESCO2):c.1044A>T (p.Gly348=)
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27787915A>T , CM000670.2:g.27787915A>T GRCh38
NC_000008.10:g.27645432A>T , CM000670.1:g.27645432A>T GRCh37
NC_000008.9:g.27701351A>T NCBI36
NG_008117.1:g.18375A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001017420.3:c.1044A>T MANE Select NP_001017420.1:p.Gly348=
ENST00000305188.13:c.1044A>T MANE Select ENSP00000306999.8:p.Gly348=
NM_001017420.2:c.1044A>T NP_001017420.1:p.Gly348=
ENST00000305188.12:c.1044A>T ENSP00000306999.8:p.Gly348=
ENST00000518262.5:c.158A>T
ENST00000522378.5:c.*19A>T ENSP00000428928.1:n.*19A>T
XM_011544421.1:c.1044A>T XP_011542723.1:p.Gly348=
XM_011544421.2:c.1044A>T XP_011542723.1:p.Gly348=
XM_011544422.1:c.1044A>T XP_011542724.1:p.Gly348=
XM_011544422.2:c.1044A>T XP_011542724.1:p.Gly348=
XR_949378.1:n.1128A>T
XR_949378.3:n.1128A>T
XR_949379.1:n.1128A>T