Canonical Allele Identifier: CA370821993
Community Standard Title: NM_001017420.3(ESCO2):c.956-2A>G
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27783998A>G , CM000670.2:g.27783998A>G GRCh38
NC_000008.10:g.27641515A>G , CM000670.1:g.27641515A>G GRCh37
NC_000008.9:g.27697434A>G NCBI36
NG_008117.1:g.14458A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001017420.3:c.956-2A>G MANE Select NP_001017420.1:n.956-2A>G
ENST00000305188.13:c.956-2A>G MANE Select ENSP00000306999.8:n.956-2A>G
NM_001017420.2:c.956-2A>G NP_001017420.1:n.956-2A>G
ENST00000305188.12:c.956-2A>G ENSP00000306999.8:n.956-2A>G
ENST00000518262.5:c.70-2A>G
ENST00000522378.5:c.862-3887A>G ENSP00000428928.1:n.862-3887A>G
XM_011544421.1:c.956-2A>G XP_011542723.1:n.956-2A>G
XM_011544421.2:c.956-2A>G XP_011542723.1:n.956-2A>G
XM_011544422.1:c.956-2A>G XP_011542724.1:n.956-2A>G
XM_011544422.2:c.956-2A>G XP_011542724.1:n.956-2A>G
XR_949378.1:n.1040-2A>G
XR_949378.3:n.1040-2A>G
XR_949379.1:n.1040-2A>G