Canonical Allele Identifier: CA2779511707
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27780283C>T , CM000670.2:g.27780283C>T GRCh38
NC_000008.10:g.27637800C>T , CM000670.1:g.27637800C>T GRCh37
NC_000008.9:g.27693719C>T NCBI36
NG_008117.1:g.10743C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305188.13:c.955+16C>T MANE Select ENSP00000306999.8:n.955+16C>T
ENST00000305188.12:c.955+16C>T ENSP00000306999.8:n.955+16C>T
ENST00000518262.5:c.69+16C>T
ENST00000522378.5:c.861+3114C>T ENSP00000428928.1:n.861+3114C>T
NM_001017420.2:c.955+16C>T NP_001017420.1:n.955+16C>T
XM_011544421.1:c.955+16C>T XP_011542723.1:n.955+16C>T
XM_011544422.1:c.955+16C>T XP_011542724.1:n.955+16C>T
XR_949378.1:n.1039+16C>T
XR_949379.1:n.1039+16C>T
XM_011544421.2:c.955+16C>T XP_011542723.1:n.955+16C>T
XM_011544422.2:c.955+16C>T XP_011542724.1:n.955+16C>T
XR_949378.3:n.1039+16C>T
NM_001017420.3:c.955+16C>T MANE Select NP_001017420.1:n.955+16C>T