Canonical Allele Identifier: CA457109464

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557799A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917354A>G , CM000669.2:g.107917354A>G	GRCh38
NC_000007.13:g.107557799A>G , CM000669.1:g.107557799A>G	GRCh37
NC_000007.12:g.107345035A>G	NCBI36
NG_008045.1:g.31214A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1128A>G MANE Select	ENSP00000205402.3:p.Gly376=
ENST00000205402.9:c.1128A>G	ENSP00000205402.3:p.Gly376=
ENST00000415325.5:c.*802A>G	ENSP00000402593.1:n.*802A>G
ENST00000417551.5:c.1128A>G	ENSP00000390667.1:p.Gly376=
ENST00000437604.6:c.984A>G	ENSP00000387542.2:p.Gly328=
ENST00000440410.5:c.1059A>G	ENSP00000417016.1:p.Gly353=
NM_000108.4:c.1128A>G	NP_000099.2:p.Gly376=
NM_001289750.1:c.831A>G	NP_001276679.1:p.Gly277=
NM_001289751.1:c.1059A>G	NP_001276680.1:p.Gly353=
NM_001289752.1:c.984A>G	NP_001276681.1:p.Gly328=
NM_000108.5:c.1128A>G MANE Select	NP_000099.2:p.Gly376=