Canonical Allele Identifier: CA1732852038
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2031632317

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107893193_107893194insA , CM000669.2:g.107893193_107893194insA GRCh38
NC_000007.13:g.107533638_107533639insA , CM000669.1:g.107533638_107533639insA GRCh37
NC_000007.12:g.107320874_107320875insA NCBI36
NG_008045.1:g.7053_7054insA

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.40-7_40-6insA MANE Select ENSP00000205402.3:n.40-7_40-6insA
ENST00000639772.1:c.40-7_40-6insA ENSP00000492159.1:n.40-7_40-6insA
ENST00000205402.9:c.40-7_40-6insA ENSP00000205402.3:n.40-7_40-6insA
ENST00000415325.5:c.40-7_40-6insA ENSP00000402593.1:n.40-7_40-6insA
ENST00000417551.5:c.40-7_40-6insA ENSP00000390667.1:n.40-7_40-6insA
ENST00000437604.6:c.40-7_40-6insA ENSP00000387542.2:n.40-7_40-6insA
ENST00000440410.5:c.40-7_40-6insA ENSP00000417016.1:n.40-7_40-6insA
ENST00000450038.5:c.40-7_40-6insA ENSP00000409590.1:n.40-7_40-6insA
ENST00000451081.5:c.40-7_40-6insA ENSP00000388077.1:n.40-7_40-6insA
ENST00000453354.5:n.105-7_105-6insA
ENST00000460577.5:n.74-7_74-6insA
ENST00000485066.1:n.129-7_129-6insA
ENST00000494441.1:n.185-7_185-6insA
NM_000108.4:c.40-7_40-6insA NP_000099.2:n.40-7_40-6insA
NM_001289750.1:c.-109-7_-109-6insA NP_001276679.1:n.-109-7_-109-6insA
NM_001289751.1:c.40-7_40-6insA NP_001276680.1:n.40-7_40-6insA
NM_001289752.1:c.40-7_40-6insA NP_001276681.1:n.40-7_40-6insA
NM_000108.5:c.40-7_40-6insA MANE Select NP_000099.2:n.40-7_40-6insA