Canonical Allele Identifier: CA580675387
Community Standard Title: NM_001017420.3(ESCO2):c.955+10A>G
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27780277A>G , CM000670.2:g.27780277A>G GRCh38
NC_000008.10:g.27637794A>G , CM000670.1:g.27637794A>G GRCh37
NC_000008.9:g.27693713A>G NCBI36
NG_008117.1:g.10737A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001017420.3:c.955+10A>G MANE Select NP_001017420.1:n.955+10A>G
ENST00000305188.13:c.955+10A>G MANE Select ENSP00000306999.8:n.955+10A>G
NM_001017420.2:c.955+10A>G NP_001017420.1:n.955+10A>G
ENST00000305188.12:c.955+10A>G ENSP00000306999.8:n.955+10A>G
ENST00000518262.5:c.69+10A>G
ENST00000522378.5:c.861+3108A>G ENSP00000428928.1:n.861+3108A>G
XM_011544421.1:c.955+10A>G XP_011542723.1:n.955+10A>G
XM_011544421.2:c.955+10A>G XP_011542723.1:n.955+10A>G
XM_011544422.1:c.955+10A>G XP_011542724.1:n.955+10A>G
XM_011544422.2:c.955+10A>G XP_011542724.1:n.955+10A>G
XR_949378.1:n.1039+10A>G
XR_949378.3:n.1039+10A>G
XR_949379.1:n.1039+10A>G