Canonical Allele Identifier: CA164246964

Gene: DLD

Linked Data

• dbSNP Id: rs765702295
• gnomAD v4: 7-107901708-CTATTT-C
• MyVariant Identifiers: chr7:g.107542154_107542158del (hg19) ; chr7:g.107901709_107901713del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107901712_107901716del , CM000669.2:g.107901712_107901716del	GRCh38
NC_000007.13:g.107542157_107542161del , CM000669.1:g.107542157_107542161del	GRCh37
NC_000007.12:g.107329393_107329397del	NCBI36
NG_008045.1:g.15572_15576del

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.119-26_119-22del MANE Select	ENSP00000205402.3:n.119-26_119-22del
ENST00000639772.1:c.119-26_119-22del	ENSP00000492159.1:n.119-26_119-22del
ENST00000205402.9:c.119-26_119-22del	ENSP00000205402.3:n.119-26_119-22del
ENST00000415325.5:c.119-1766_119-1762del	ENSP00000402593.1:n.119-1766_119-1762del
ENST00000417551.5:c.119-26_119-22del	ENSP00000390667.1:n.119-26_119-22del
ENST00000437604.6:c.119-26_119-22del	ENSP00000387542.2:n.119-26_119-22del
ENST00000440410.5:c.119-26_119-22del	ENSP00000417016.1:n.119-26_119-22del
ENST00000450038.5:c.119-26_119-22del	ENSP00000409590.1:n.119-26_119-22del
ENST00000451081.5:c.119-26_119-22del	ENSP00000388077.1:n.119-26_119-22del
ENST00000453354.5:n.184-26_184-22del
ENST00000460577.5:n.153-26_153-22del
ENST00000494441.1:n.264-26_264-22del
NM_000108.4:c.119-26_119-22del	NP_000099.2:n.119-26_119-22del
NM_001289750.1:c.-30-1766_-30-1762del	NP_001276679.1:n.-30-1766_-30-1762del
NM_001289751.1:c.119-26_119-22del	NP_001276680.1:n.119-26_119-22del
NM_001289752.1:c.119-26_119-22del	NP_001276681.1:n.119-26_119-22del
NM_000108.5:c.119-26_119-22del MANE Select	NP_000099.2:n.119-26_119-22del