Canonical Allele Identifier: CA577039422

Gene: DLD

Linked Data

• dbSNP Id: rs1214235686
• gnomAD v2: 7-107560400-TTAAA-T
• gnomAD v3: 7-107919955-TTAAA-T
• gnomAD v4: 7-107919955-TTAAA-T
• MyVariant Identifiers: chr7:g.107560401_107560404del (hg19) ; chr7:g.107919956_107919959del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919958_107919961del , CM000669.2:g.107919958_107919961del	GRCh38
NC_000007.13:g.107560403_107560406del , CM000669.1:g.107560403_107560406del	GRCh37
NC_000007.12:g.107347639_107347642del	NCBI36
NG_008045.1:g.33818_33821del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*699_*702del MANE Select	ENSP00000205402.3:n.*699_*702del
ENST00000205402.9:c.*699_*702del	ENSP00000205402.3:n.*699_*702del
ENST00000417551.5:c.*124+575_*124+578del	ENSP00000390667.1:n.*124+575_*124+578del
NM_000108.4:c.*699_*702del	NP_000099.2:n.*699_*702del
NM_001289750.1:c.*699_*702del	NP_001276679.1:n.*699_*702del
NM_001289751.1:c.*699_*702del	NP_001276680.1:n.*699_*702del
NM_001289752.1:c.*699_*702del	NP_001276681.1:n.*699_*702del
NM_000108.5:c.*699_*702del MANE Select	NP_000099.2:n.*699_*702del