Canonical Allele Identifier: CA2684459016
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917459_107917461del , CM000669.2:g.107917459_107917461del GRCh38
NC_000007.13:g.107557904_107557906del , CM000669.1:g.107557904_107557906del GRCh37
NC_000007.12:g.107345140_107345142del NCBI36
NG_008045.1:g.31319_31321del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1233_1235del MANE Select ENSP00000205402.3:p.Glu412del
ENST00000205402.9:c.1233_1235del ENSP00000205402.3:p.Glu412del
ENST00000415325.5:c.*907_*909del ENSP00000402593.1:n.*907_*909del
ENST00000417551.5:c.1233_1235del ENSP00000390667.1:p.Glu412del
ENST00000437604.6:c.1089_1091del ENSP00000387542.2:p.Glu364del
ENST00000440410.5:c.1164_1166del ENSP00000417016.1:p.Glu389del
NM_000108.4:c.1233_1235del NP_000099.2:p.Glu412del
NM_001289750.1:c.936_938del NP_001276679.1:p.Glu313del
NM_001289751.1:c.1164_1166del NP_001276680.1:p.Glu389del
NM_001289752.1:c.1089_1091del NP_001276681.1:p.Glu364del
NM_000108.5:c.1233_1235del MANE Select NP_000099.2:p.Glu412del