Canonical Allele Identifier: CA1772946665

Gene: ESCO2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27780270_27780272delinsAAG , CM000670.2:g.27780270_27780272delinsAAG	GRCh38
NC_000008.10:g.27637787_27637789delinsAAG , CM000670.1:g.27637787_27637789delinsAAG	GRCh37
NC_000008.9:g.27693706_27693708delinsAAG	NCBI36
NG_008117.1:g.10730_10732delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305188.13:c.955+3_955+5delinsAAG MANE Select	ENSP00000306999.8:n.955+3_955+5delinsAAG
ENST00000305188.12:c.955+3_955+5delinsAAG	ENSP00000306999.8:n.955+3_955+5delinsAAG
ENST00000518262.5:c.69+3_69+5delinsAAG
ENST00000522378.5:c.861+3101_861+3103delinsAAG	ENSP00000428928.1:n.861+3101_861+3103delinsAAG
NM_001017420.2:c.955+3_955+5delinsAAG	NP_001017420.1:n.955+3_955+5delinsAAG
XM_011544421.1:c.955+3_955+5delinsAAG	XP_011542723.1:n.955+3_955+5delinsAAG
XM_011544422.1:c.955+3_955+5delinsAAG	XP_011542724.1:n.955+3_955+5delinsAAG
XR_949378.1:n.1039+3_1039+5delinsAAG
XR_949379.1:n.1039+3_1039+5delinsAAG
XM_011544421.2:c.955+3_955+5delinsAAG	XP_011542723.1:n.955+3_955+5delinsAAG
XM_011544422.2:c.955+3_955+5delinsAAG	XP_011542724.1:n.955+3_955+5delinsAAG
XR_949378.3:n.1039+3_1039+5delinsAAG
NM_001017420.3:c.955+3_955+5delinsAAG MANE Select	NP_001017420.1:n.955+3_955+5delinsAAG