Canonical Allele Identifier: CA2533444413

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917229_107917232del , CM000669.2:g.107917229_107917232del	GRCh38
NC_000007.13:g.107557674_107557677del , CM000669.1:g.107557674_107557677del	GRCh37
NC_000007.12:g.107344910_107344913del	NCBI36
NG_008045.1:g.31089_31092del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1047-44_1047-41del MANE Select	ENSP00000205402.3:n.1047-44_1047-41del
ENST00000205402.9:c.1047-44_1047-41del	ENSP00000205402.3:n.1047-44_1047-41del
ENST00000415325.5:c.*721-44_*721-41del	ENSP00000402593.1:n.*721-44_*721-41del
ENST00000417551.5:c.1047-44_1047-41del	ENSP00000390667.1:n.1047-44_1047-41del
ENST00000437604.6:c.903-44_903-41del	ENSP00000387542.2:n.903-44_903-41del
ENST00000440410.5:c.978-44_978-41del	ENSP00000417016.1:n.978-44_978-41del
NM_000108.4:c.1047-44_1047-41del	NP_000099.2:n.1047-44_1047-41del
NM_001289750.1:c.750-44_750-41del	NP_001276679.1:n.750-44_750-41del
NM_001289751.1:c.978-44_978-41del	NP_001276680.1:n.978-44_978-41del
NM_001289752.1:c.903-44_903-41del	NP_001276681.1:n.903-44_903-41del
NM_000108.5:c.1047-44_1047-41del MANE Select	NP_000099.2:n.1047-44_1047-41del