Canonical Allele Identifier: CA1105646258

Gene: DLD

Linked Data

• dbSNP Id: rs2032378578
• gnomAD v3: 7-107920273-G-T
• gnomAD v4: 7-107920273-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107920273G>T , CM000669.2:g.107920273G>T	GRCh38
NC_000007.13:g.107560718G>T , CM000669.1:g.107560718G>T	GRCh37
NC_000007.12:g.107347954G>T	NCBI36
NG_008045.1:g.34133G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.*1014G>T MANE Select	ENSP00000205402.3:n.*1014G>T
ENST00000205402.9:c.*1014G>T	ENSP00000205402.3:n.*1014G>T
ENST00000417551.5:c.*124+890G>T	ENSP00000390667.1:n.*124+890G>T
NM_000108.4:c.*1014G>T	NP_000099.2:n.*1014G>T
NM_001289750.1:c.*1014G>T	NP_001276679.1:n.*1014G>T
NM_001289751.1:c.*1014G>T	NP_001276680.1:n.*1014G>T
NM_001289752.1:c.*1014G>T	NP_001276681.1:n.*1014G>T
NM_000108.5:c.*1014G>T MANE Select	NP_000099.2:n.*1014G>T