Canonical Allele Identifier: CA2684462801
Gene: DLD HGNC NCBI

Linked Data

gnomAD v4: 7-107920247-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920247G>T , CM000669.2:g.107920247G>T GRCh38
NC_000007.13:g.107560692G>T , CM000669.1:g.107560692G>T GRCh37
NC_000007.12:g.107347928G>T NCBI36
NG_008045.1:g.34107G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*988G>T MANE Select ENSP00000205402.3:n.*988G>T
ENST00000205402.9:c.*988G>T ENSP00000205402.3:n.*988G>T
ENST00000417551.5:c.*124+864G>T ENSP00000390667.1:n.*124+864G>T
NM_000108.4:c.*988G>T NP_000099.2:n.*988G>T
NM_001289750.1:c.*988G>T NP_001276679.1:n.*988G>T
NM_001289751.1:c.*988G>T NP_001276680.1:n.*988G>T
NM_001289752.1:c.*988G>T NP_001276681.1:n.*988G>T
NM_000108.5:c.*988G>T MANE Select NP_000099.2:n.*988G>T
Search 100 bp 5'
Search 100 bp 3'