Canonical Allele Identifier: CA577037221

Gene: DLD

Linked Data

• dbSNP Id: rs1206033620
• gnomAD v2: 7-107533630-ATTTTCT-A
• gnomAD v4: 7-107893185-ATTTTCT-A
• MyVariant Identifiers: chr7:g.107533631_107533636del (hg19) ; chr7:g.107893186_107893191del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893192_107893197del , CM000669.2:g.107893192_107893197del	GRCh38
NC_000007.13:g.107533637_107533642del , CM000669.1:g.107533637_107533642del	GRCh37
NC_000007.12:g.107320873_107320878del	NCBI36
NG_008045.1:g.7052_7057del

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.40-8_40-3del MANE Select	ENSP00000205402.3:n.40-8_40-3del
ENST00000639772.1:c.40-8_40-3del	ENSP00000492159.1:n.40-8_40-3del
ENST00000205402.9:c.40-8_40-3del	ENSP00000205402.3:n.40-8_40-3del
ENST00000415325.5:c.40-8_40-3del	ENSP00000402593.1:n.40-8_40-3del
ENST00000417551.5:c.40-8_40-3del	ENSP00000390667.1:n.40-8_40-3del
ENST00000437604.6:c.40-8_40-3del	ENSP00000387542.2:n.40-8_40-3del
ENST00000440410.5:c.40-8_40-3del	ENSP00000417016.1:n.40-8_40-3del
ENST00000450038.5:c.40-8_40-3del	ENSP00000409590.1:n.40-8_40-3del
ENST00000451081.5:c.40-8_40-3del	ENSP00000388077.1:n.40-8_40-3del
ENST00000453354.5:n.105-8_105-3del
ENST00000460577.5:n.74-8_74-3del
ENST00000485066.1:n.129-8_129-3del
ENST00000494441.1:n.185-8_185-3del
NM_000108.4:c.40-8_40-3del	NP_000099.2:n.40-8_40-3del
NM_001289750.1:c.-109-8_-109-3del	NP_001276679.1:n.-109-8_-109-3del
NM_001289751.1:c.40-8_40-3del	NP_001276680.1:n.40-8_40-3del
NM_001289752.1:c.40-8_40-3del	NP_001276681.1:n.40-8_40-3del
NM_000108.5:c.40-8_40-3del MANE Select	NP_000099.2:n.40-8_40-3del