Canonical Allele Identifier: CA577039425

Gene: DLD

Linked Data

• dbSNP Id: rs1175970997
• gnomAD v2: 7-107560487-CT-C
• gnomAD v3: 7-107920042-CT-C
• gnomAD v4: 7-107920042-CT-C
• MyVariant Identifiers: chr7:g.107560488del (hg19) ; chr7:g.107920043del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107920046del , CM000669.2:g.107920046del	GRCh38
NC_000007.13:g.107560491del , CM000669.1:g.107560491del	GRCh37
NC_000007.12:g.107347727del	NCBI36
NG_008045.1:g.33906del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*787del MANE Select	ENSP00000205402.3:n.*787del
ENST00000205402.9:c.*787del	ENSP00000205402.3:n.*787del
ENST00000417551.5:c.*124+663del	ENSP00000390667.1:n.*124+663del
NM_000108.4:c.*787del	NP_000099.2:n.*787del
NM_001289750.1:c.*787del	NP_001276679.1:n.*787del
NM_001289751.1:c.*787del	NP_001276680.1:n.*787del
NM_001289752.1:c.*787del	NP_001276681.1:n.*787del
NM_000108.5:c.*787del MANE Select	NP_000099.2:n.*787del