Canonical Allele Identifier: CA4434367

Gene: DLD

Linked Data

• dbSNP Id: rs758973358
• ExAC: 7:107542148 AT / A
• gnomAD v2: 7-107542148-AT-A
• gnomAD v4: 7-107901703-AT-A
• MyVariant Identifiers: chr7:g.107542149del (hg19) ; chr7:g.107901704del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107901706del , CM000669.2:g.107901706del	GRCh38
NC_000007.13:g.107542151del , CM000669.1:g.107542151del	GRCh37
NC_000007.12:g.107329387del	NCBI36
NG_008045.1:g.15566del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.119-32del MANE Select	ENSP00000205402.3:n.119-32del
ENST00000639772.1:c.119-32del	ENSP00000492159.1:n.119-32del
ENST00000205402.9:c.119-32del	ENSP00000205402.3:n.119-32del
ENST00000415325.5:c.119-1772del	ENSP00000402593.1:n.119-1772del
ENST00000417551.5:c.119-32del	ENSP00000390667.1:n.119-32del
ENST00000437604.6:c.119-32del	ENSP00000387542.2:n.119-32del
ENST00000440410.5:c.119-32del	ENSP00000417016.1:n.119-32del
ENST00000450038.5:c.119-32del	ENSP00000409590.1:n.119-32del
ENST00000451081.5:c.119-32del	ENSP00000388077.1:n.119-32del
ENST00000453354.5:n.184-32del
ENST00000460577.5:n.153-32del
ENST00000494441.1:n.264-32del
NM_000108.4:c.119-32del	NP_000099.2:n.119-32del
NM_001289750.1:c.-30-1772del	NP_001276679.1:n.-30-1772del
NM_001289751.1:c.119-32del	NP_001276680.1:n.119-32del
NM_001289752.1:c.119-32del	NP_001276681.1:n.119-32del
NM_000108.5:c.119-32del MANE Select	NP_000099.2:n.119-32del