Canonical Allele Identifier: CA2684476687
Gene: DLD HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107893264_107893265insAA , CM000669.2:g.107893264_107893265insAA GRCh38
NC_000007.13:g.107533709_107533710insAA , CM000669.1:g.107533709_107533710insAA GRCh37
NC_000007.12:g.107320945_107320946insAA NCBI36
NG_008045.1:g.7124_7125insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.104_105insAA MANE Select ENSP00000205402.3:p.Tyr35Ter
ENST00000639772.1:c.104_105insAA ENSP00000492159.1:p.Tyr35Ter
ENST00000205402.9:c.104_105insAA ENSP00000205402.3:p.Tyr35Ter
ENST00000415325.5:c.104_105insAA ENSP00000402593.1:p.Tyr35Ter
ENST00000417551.5:c.104_105insAA ENSP00000390667.1:p.Tyr35Ter
ENST00000437604.6:c.104_105insAA ENSP00000387542.2:p.Tyr35Ter
ENST00000440410.5:c.104_105insAA ENSP00000417016.1:p.Tyr35Ter
ENST00000450038.5:c.104_105insAA ENSP00000409590.1:p.Tyr35Ter
ENST00000451081.5:c.104_105insAA ENSP00000388077.1:p.Tyr35Ter
ENST00000453354.5:n.169_170insAA
ENST00000460577.5:n.138_139insAA
ENST00000485066.1:n.193_194insAA
ENST00000494441.1:n.249_250insAA
NM_000108.4:c.104_105insAA NP_000099.2:p.Tyr35Ter
NM_001289750.1:c.-45_-44insAA NP_001276679.1:n.-45_-44insAA
NM_001289751.1:c.104_105insAA NP_001276680.1:p.Tyr35Ter
NM_001289752.1:c.104_105insAA NP_001276681.1:p.Tyr35Ter
NM_000108.5:c.104_105insAA MANE Select NP_000099.2:p.Tyr35Ter