Canonical Allele Identifier: CA577039457

Gene: DLD

Linked Data

• dbSNP Id: rs1378589820
• gnomAD v2: 7-107560662-GACTGTTTATTTAAA-G
• gnomAD v3: 7-107920217-GACTGTTTATTTAAA-G
• gnomAD v4: 7-107920217-GACTGTTTATTTAAA-G
• MyVariant Identifiers: chr7:g.107560663_107560676del (hg19) ; chr7:g.107920218_107920231del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107920218_107920231del , CM000669.2:g.107920218_107920231del	GRCh38
NC_000007.13:g.107560663_107560676del , CM000669.1:g.107560663_107560676del	GRCh37
NC_000007.12:g.107347899_107347912del	NCBI36
NG_008045.1:g.34078_34091del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*959_*972del MANE Select	ENSP00000205402.3:n.*959_*972del
ENST00000205402.9:c.*959_*972del	ENSP00000205402.3:n.*959_*972del
ENST00000417551.5:c.*124+835_*124+848del	ENSP00000390667.1:n.*124+835_*124+848del
NM_000108.4:c.*959_*972del	NP_000099.2:n.*959_*972del
NM_001289750.1:c.*959_*972del	NP_001276679.1:n.*959_*972del
NM_001289751.1:c.*959_*972del	NP_001276680.1:n.*959_*972del
NM_001289752.1:c.*959_*972del	NP_001276681.1:n.*959_*972del
NM_000108.5:c.*959_*972del MANE Select	NP_000099.2:n.*959_*972del