Canonical Allele Identifier: CA2619235438
Community Standard Title: NM_001345.5(DGKA):c.710-251del
Gene: DGKA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55939831del , CM000674.2:g.55939831del GRCh38
NC_000012.11:g.56333615del , CM000674.1:g.56333615del GRCh37
NC_000012.10:g.54619882del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001345.5:c.710-251del MANE Select NP_001336.2:n.710-251del
ENST00000331886.10:c.710-251del MANE Select ENSP00000328405.5:n.710-251del
NM_001345.4:c.710-251del NP_001336.2:n.710-251del
NM_001351033.1:c.710-251del NP_001337962.1:n.710-251del
NM_001351033.2:c.710-251del NP_001337962.1:n.710-251del
NM_001351034.1:c.710-251del NP_001337963.1:n.710-251del
NM_001351034.2:c.710-251del NP_001337963.1:n.710-251del
NM_001351035.1:c.824-251del NP_001337964.1:n.824-251del
NM_001351036.1:c.287-251del NP_001337965.1:n.287-251del
NM_001351036.2:c.287-251del NP_001337965.1:n.287-251del
NM_001351037.1:c.287-251del NP_001337966.1:n.287-251del
NM_001351038.1:c.-265+302del NP_001337967.1:n.-265+302del
NM_001351038.2:c.-265+302del NP_001337967.1:n.-265+302del
NM_001351039.1:c.-265+302del NP_001337968.1:n.-265+302del
NM_001351039.2:c.-265+302del NP_001337968.1:n.-265+302del
NM_001351040.1:c.-265+302del NP_001337969.1:n.-265+302del
NM_001351040.2:c.-265+302del NP_001337969.1:n.-265+302del
NM_201444.2:c.710-251del NP_958852.1:n.710-251del
NM_201444.3:c.710-251del NP_958852.1:n.710-251del
NM_201445.1:c.710-251del NP_958853.1:n.710-251del
NM_201445.2:c.710-251del NP_958853.1:n.710-251del
NM_201554.1:c.710-251del NP_963848.1:n.710-251del
NM_201554.2:c.710-251del NP_963848.1:n.710-251del
NR_147026.1:n.887-251del
NR_147026.2:n.852-251del
NR_147027.1:n.1130-251del
NR_147027.2:n.1095-251del
ENST00000331886.9:c.710-251del ENSP00000328405.5:n.710-251del
ENST00000394147.5:c.710-251del ENSP00000377703.1:n.710-251del
ENST00000402956.7:c.709+302del ENSP00000385792.3:n.709+302del
ENST00000547358.5:n.837-251del
ENST00000548047.5:n.589del
ENST00000549079.6:n.436-251del
ENST00000549097.5:n.1164del
ENST00000549986.5:n.478-251del
ENST00000551156.5:c.710-251del ENSP00000450359.1:n.710-251del
ENST00000551296.5:n.2327-251del
ENST00000551739.5:n.1268del
ENST00000552335.6:n.423-251del
ENST00000552478.5:n.2524-251del
ENST00000552652.2:n.44-251del
ENST00000552687.6:n.635del
ENST00000553084.5:c.*364-251del ENSP00000446605.1:n.*364-251del
ENST00000554434.6:n.141-251del
ENST00000555218.5:c.467-251del ENSP00000451743.1:n.467-251del
ENST00000557180.5:c.56-251del ENSP00000451330.1:n.56-251del
XM_005268688.1:c.824-251del XP_005268745.1:n.824-251del
XM_005268689.1:c.374-251del XP_005268746.1:n.374-251del
XM_005268689.2:c.374-251del XP_005268746.1:n.374-251del
XM_005268690.1:c.374-251del XP_005268747.1:n.374-251del
XM_011537990.1:c.824-251del XP_011536292.1:n.824-251del
XM_011537991.1:c.710-251del XP_011536293.1:n.710-251del
XM_011537992.1:c.710-251del XP_011536294.1:n.710-251del
XM_011537993.1:c.710-251del XP_011536295.1:n.710-251del
XM_011537993.2:c.710-251del XP_011536295.1:n.710-251del
XM_011537994.1:c.473-251del XP_011536296.1:n.473-251del
XM_011537995.1:c.374-251del XP_011536297.1:n.374-251del
XM_011537995.2:c.374-251del XP_011536297.1:n.374-251del
XM_017018900.1:c.1178-251del XP_016874389.1:n.1178-251del
XM_017018901.2:c.1064-251del XP_016874390.1:n.1064-251del
XM_017018902.1:c.1064-251del XP_016874391.1:n.1064-251del
XM_017018903.1:c.1064-251del XP_016874392.1:n.1064-251del
XM_017018904.1:c.1064-251del XP_016874393.1:n.1064-251del
XM_017018905.1:c.1064-251del XP_016874394.1:n.1064-251del
XM_017018906.2:c.1064-251del XP_016874395.1:n.1064-251del
XM_017018907.1:c.1064-251del XP_016874396.1:n.1064-251del
XM_017018908.1:c.962-251del XP_016874397.1:n.962-251del
XR_001748602.1:n.1270-251del
XR_002957293.1:n.1270-251del
XR_002957294.1:n.916-251del
XR_002957295.1:n.1269+302del
XR_002957296.1:n.881-251del
XR_429084.2:n.916-251del