Canonical Allele Identifier: CA2686704265
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27777066_27777068del , CM000670.2:g.27777066_27777068del GRCh38
NC_000008.10:g.27634583_27634585del , CM000670.1:g.27634583_27634585del GRCh37
NC_000008.9:g.27690502_27690504del NCBI36
NG_008117.1:g.7526_7528del

Transcript Alleles

HGVS Amino-acid Change
NM_001017420.3:c.758_760del MANE Select NP_001017420.1:p.Lys253del
ENST00000305188.13:c.758_760del MANE Select ENSP00000306999.8:p.Lys253del
NM_001017420.2:c.758_760del NP_001017420.1:p.Lys253del
ENST00000305188.12:c.758_760del ENSP00000306999.8:p.Lys253del
ENST00000522378.5:c.758_760del ENSP00000428928.1:p.Lys253del
ENST00000523910.1:n.557_559del
ENST00000524293.1:n.776_778del
XM_011544421.1:c.758_760del XP_011542723.1:p.Lys253del
XM_011544421.2:c.758_760del XP_011542723.1:p.Lys253del
XM_011544422.1:c.758_760del XP_011542724.1:p.Lys253del
XM_011544422.2:c.758_760del XP_011542724.1:p.Lys253del
XR_949378.1:n.842_844del
XR_949378.3:n.842_844del
XR_949379.1:n.842_844del