Canonical Allele Identifier: CA831211544

Gene: DLD

Linked Data

• dbSNP Id: rs1303754938
• MyVariant Identifiers: chr7:g.107560421_107560423del (hg19) ; chr7:g.107919976_107919978del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919978_107919980del , CM000669.2:g.107919978_107919980del	GRCh38
NC_000007.13:g.107560423_107560425del , CM000669.1:g.107560423_107560425del	GRCh37
NC_000007.12:g.107347659_107347661del	NCBI36
NG_008045.1:g.33838_33840del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*719_*721del MANE Select	ENSP00000205402.3:n.*719_*721del
ENST00000205402.9:c.*719_*721del	ENSP00000205402.3:n.*719_*721del
ENST00000417551.5:c.*124+595_*124+597del	ENSP00000390667.1:n.*124+595_*124+597del
NM_000108.4:c.*719_*721del	NP_000099.2:n.*719_*721del
NM_001289750.1:c.*719_*721del	NP_001276679.1:n.*719_*721del
NM_001289751.1:c.*719_*721del	NP_001276680.1:n.*719_*721del
NM_001289752.1:c.*719_*721del	NP_001276681.1:n.*719_*721del
NM_000108.5:c.*719_*721del MANE Select	NP_000099.2:n.*719_*721del