Canonical Allele Identifier: CA341789
Gene: ESCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 21243
dbSNP Id: rs80359846

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27776615_27776619del , CM000670.2:g.27776615_27776619del GRCh38
NC_000008.10:g.27634132_27634136del , CM000670.1:g.27634132_27634136del GRCh37
NC_000008.9:g.27690051_27690055del NCBI36
NG_008117.1:g.7075_7079del

Transcript Alleles

HGVS Amino-acid change
ENST00000305188.13:c.307_311del MANE Select ENSP00000306999.8:p.Lys103GlufsTer2
ENST00000305188.12:c.307_311del ENSP00000306999.8:p.Lys103GlufsTer2
ENST00000519637.1:c.307_311del ENSP00000428027.1:p.Lys103GlufsTer2
ENST00000522378.5:c.307_311del ENSP00000428928.1:p.Lys103GlufsTer2
ENST00000523566.5:c.307_311del ENSP00000428435.1:p.Lys103GlufsTer2
ENST00000523910.1:n.106_110del
ENST00000524293.1:n.325_329del
NM_001017420.2:c.307_311del NP_001017420.1:p.Lys103GlufsTer2
XM_011544421.1:c.307_311del XP_011542723.1:p.Lys103GlufsTer2
XM_011544422.1:c.307_311del XP_011542724.1:p.Lys103GlufsTer2
XR_949378.1:n.391_395del
XR_949379.1:n.391_395del
XM_011544421.2:c.307_311del XP_011542723.1:p.Lys103GlufsTer2
XM_011544422.2:c.307_311del XP_011542724.1:p.Lys103GlufsTer2
XR_949378.3:n.391_395del
NM_001017420.3:c.307_311del MANE Select NP_001017420.1:p.Lys103GlufsTer2