Canonical Allele Identifier: CA370820049
Community Standard Title: NM_001017420.3(ESCO2):c.861+1G>A
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27777170G>A , CM000670.2:g.27777170G>A GRCh38
NC_000008.10:g.27634687G>A , CM000670.1:g.27634687G>A GRCh37
NC_000008.9:g.27690606G>A NCBI36
NG_008117.1:g.7630G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001017420.3:c.861+1G>A MANE Select NP_001017420.1:n.861+1G>A
ENST00000305188.13:c.861+1G>A MANE Select ENSP00000306999.8:n.861+1G>A
NM_001017420.2:c.861+1G>A NP_001017420.1:n.861+1G>A
ENST00000305188.12:c.861+1G>A ENSP00000306999.8:n.861+1G>A
ENST00000522378.5:c.861+1G>A ENSP00000428928.1:n.861+1G>A
ENST00000523910.1:n.660+1G>A
ENST00000524293.1:n.880G>A
XM_011544421.1:c.861+1G>A XP_011542723.1:n.861+1G>A
XM_011544421.2:c.861+1G>A XP_011542723.1:n.861+1G>A
XM_011544422.1:c.861+1G>A XP_011542724.1:n.861+1G>A
XM_011544422.2:c.861+1G>A XP_011542724.1:n.861+1G>A
XR_949378.1:n.945+1G>A
XR_949378.3:n.945+1G>A
XR_949379.1:n.945+1G>A