Canonical Allele Identifier: CA1772997924
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27803304A= , CM000670.2:g.27803304A= GRCh38
NC_000008.10:g.27660821A= , CM000670.1:g.27660821A= GRCh37
NC_000008.9:g.27716740A= NCBI36
NG_008117.1:g.33764A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305188.13:c.1674-2A= MANE Select ENSP00000306999.8:n.1674-2A=
ENST00000305188.12:c.1674-2A= ENSP00000306999.8:n.1674-2A=
ENST00000397418.4:c.618-2A= ENSP00000380563.2:n.618-2A=
ENST00000522378.5:c.*649-2A= ENSP00000428928.1:n.*649-2A=
NM_001017420.2:c.1674-2A= NP_001017420.1:n.1674-2A=
XM_011544421.1:c.1674-2A= XP_011542723.1:n.1674-2A=
XM_011544422.1:c.1674-2A= XP_011542724.1:n.1674-2A=
XR_949378.1:n.1758-2A=
XR_949379.1:n.1758-2A=
XM_011544421.2:c.1674-2A= XP_011542723.1:n.1674-2A=
XM_011544422.2:c.1674-2A= XP_011542724.1:n.1674-2A=
XR_949378.3:n.1758-2A=
NM_001017420.3:c.1674-2A= MANE Select NP_001017420.1:n.1674-2A=