Canonical Allele Identifier: CA1772946661
Gene: ESCO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.27780265_27780269delinsCAAGT , CM000670.2:g.27780265_27780269delinsCAAGT GRCh38
NC_000008.10:g.27637782_27637786delinsCAAGT , CM000670.1:g.27637782_27637786delinsCAAGT GRCh37
NC_000008.9:g.27693701_27693705delinsCAAGT NCBI36
NG_008117.1:g.10725_10729delinsCAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000305188.13:c.953_955+2delinsCAAGT
ENST00000305188.12:c.953_955+2delinsCAAGT
ENST00000518262.5:c.67_69+2delinsCAAGT
ENST00000522378.5:c.861+3096_861+3100delinsCAAGT ENSP00000428928.1:n.861+3096_861+3100delinsCAAGT
NM_001017420.2:c.953_955+2delinsCAAGT
XM_011544421.1:c.953_955+2delinsCAAGT
XM_011544422.1:c.953_955+2delinsCAAGT
XR_949378.1:n.1037_1039+2delinsCAAGT
XR_949379.1:n.1037_1039+2delinsCAAGT
XM_011544421.2:c.953_955+2delinsCAAGT
XM_011544422.2:c.953_955+2delinsCAAGT
XR_949378.3:n.1037_1039+2delinsCAAGT
NM_001017420.3:c.953_955+2delinsCAAGT