Canonical Allele Identifier: CA658821779

Gene: DLD

Linked Data

• ClinVar Variation Id: 558106
• ClinVar RCV Id: RCV000674332
• dbSNP Id: rs1554400720
• MyVariant Identifiers: chr7:g.107919098del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919098del , CM000669.2:g.107919098del	GRCh38
NC_000007.13:g.107559543del , CM000669.1:g.107559543del	GRCh37
NC_000007.12:g.107346779del	NCBI36
NG_008045.1:g.32958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1463del MANE Select	ENSP00000205402.3:p.Pro488ArgfsTer?
ENST00000205402.9:c.1463del	ENSP00000205402.3:p.Pro488ArgfsTer?
ENST00000415325.5:c.*1137del	ENSP00000402593.1:n.*1137del
ENST00000417551.5:c.1463del	ENSP00000390667.1:p.Pro488ArgfsTer?
ENST00000437604.6:c.1319del	ENSP00000387542.2:p.Pro440ArgfsTer?
ENST00000440410.5:c.1394del	ENSP00000417016.1:p.Pro465ArgfsTer?
NM_000108.4:c.1463del	NP_000099.2:p.Pro488ArgfsTer?
NM_001289750.1:c.1166del	NP_001276679.1:p.Pro389ArgfsTer?
NM_001289751.1:c.1394del	NP_001276680.1:p.Pro465ArgfsTer?
NM_001289752.1:c.1319del	NP_001276681.1:p.Pro440ArgfsTer?
NM_000108.5:c.1463del MANE Select	NP_000099.2:p.Pro488ArgfsTer?