Canonical Allele Identifier: CA1732859986

Gene: DLD

Linked Data

• dbSNP Id: rs2032290300
• gnomAD v4: 7-107917149-AGAGCTGCATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917152_107917162del , CM000669.2:g.107917152_107917162del	GRCh38
NC_000007.13:g.107557597_107557607del , CM000669.1:g.107557597_107557607del	GRCh37
NC_000007.12:g.107344833_107344843del	NCBI36
NG_008045.1:g.31012_31022del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1047-121_1047-111del MANE Select	ENSP00000205402.3:n.1047-121_1047-111del
ENST00000205402.9:c.1047-121_1047-111del	ENSP00000205402.3:n.1047-121_1047-111del
ENST00000415325.5:c.*721-121_*721-111del	ENSP00000402593.1:n.*721-121_*721-111del
ENST00000417551.5:c.1047-121_1047-111del	ENSP00000390667.1:n.1047-121_1047-111del
ENST00000437604.6:c.903-121_903-111del	ENSP00000387542.2:n.903-121_903-111del
ENST00000440410.5:c.978-121_978-111del	ENSP00000417016.1:n.978-121_978-111del
NM_000108.4:c.1047-121_1047-111del	NP_000099.2:n.1047-121_1047-111del
NM_001289750.1:c.750-121_750-111del	NP_001276679.1:n.750-121_750-111del
NM_001289751.1:c.978-121_978-111del	NP_001276680.1:n.978-121_978-111del
NM_001289752.1:c.903-121_903-111del	NP_001276681.1:n.903-121_903-111del
NM_000108.5:c.1047-121_1047-111del MANE Select	NP_000099.2:n.1047-121_1047-111del