Canonical Allele Identifier: CA368858638
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917455A>T , CM000669.2:g.107917455A>T GRCh38
NC_000007.13:g.107557900A>T , CM000669.1:g.107557900A>T GRCh37
NC_000007.12:g.107345136A>T NCBI36
NG_008045.1:g.31315A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1229A>T MANE Select ENSP00000205402.3:p.Lys410Ile
ENST00000205402.9:c.1229A>T ENSP00000205402.3:p.Lys410Ile
ENST00000415325.5:c.*903A>T ENSP00000402593.1:n.*903A>T
ENST00000417551.5:c.1229A>T ENSP00000390667.1:p.Lys410Ile
ENST00000437604.6:c.1085A>T ENSP00000387542.2:p.Lys362Ile
ENST00000440410.5:c.1160A>T ENSP00000417016.1:p.Lys387Ile
NM_000108.4:c.1229A>T NP_000099.2:p.Lys410Ile
NM_001289750.1:c.932A>T NP_001276679.1:p.Lys311Ile
NM_001289751.1:c.1160A>T NP_001276680.1:p.Lys387Ile
NM_001289752.1:c.1085A>T NP_001276681.1:p.Lys362Ile
NM_000108.5:c.1229A>T MANE Select NP_000099.2:p.Lys410Ile