Canonical Allele Identifier: CA2038177218

Gene: DGKA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55954020_55954024delinsCTAAG , CM000674.2:g.55954020_55954024delinsCTAAG	GRCh38
NC_000012.11:g.56347804_56347808delinsCTAAG , CM000674.1:g.56347804_56347808delinsCTAAG	GRCh37
NC_000012.10:g.54634071_54634075delinsCTAAG	NCBI36
NG_028086.1:g.17689_17693delinsCTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402956.7:c.*1627_*1631delinsCTAAG	ENSP00000385792.3:n.*1627_*1631delinsCTAAG
ENST00000551156.5:c.*252_*256delinsCTAAG	ENSP00000450359.1:n.*252_*256delinsCTAAG
XM_005268688.1:c.*252_*256delinsCTAAG	XP_005268745.1:n.*252_*256delinsCTAAG
XM_005268689.1:c.*252_*256delinsCTAAG	XP_005268746.1:n.*252_*256delinsCTAAG
XM_005268690.1:c.*252_*256delinsCTAAG	XP_005268747.1:n.*252_*256delinsCTAAG
XM_011537990.1:c.*252_*256delinsCTAAG	XP_011536292.1:n.*252_*256delinsCTAAG
XM_011537991.1:c.*252_*256delinsCTAAG	XP_011536293.1:n.*252_*256delinsCTAAG
XM_011537992.1:c.*252_*256delinsCTAAG	XP_011536294.1:n.*252_*256delinsCTAAG
XM_011537993.1:c.*252_*256delinsCTAAG	XP_011536295.1:n.*252_*256delinsCTAAG
XM_011537994.1:c.*252_*256delinsCTAAG	XP_011536296.1:n.*252_*256delinsCTAAG
XM_011537995.1:c.*252_*256delinsCTAAG	XP_011536297.1:n.*252_*256delinsCTAAG