Canonical Allele Identifier: CA368857772

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557353A>T (hg19) ; chr7:g.107916908A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916908A>T , CM000669.2:g.107916908A>T	GRCh38
NC_000007.13:g.107557353A>T , CM000669.1:g.107557353A>T	GRCh37
NC_000007.12:g.107344589A>T	NCBI36
NG_008045.1:g.30768A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.990A>T MANE Select	ENSP00000205402.3:p.Glu330Asp
ENST00000205402.9:c.990A>T	ENSP00000205402.3:p.Glu330Asp
ENST00000415325.5:c.*664A>T	ENSP00000402593.1:n.*664A>T
ENST00000417551.5:c.990A>T	ENSP00000390667.1:p.Glu330Asp
ENST00000437604.6:c.846A>T	ENSP00000387542.2:p.Glu282Asp
ENST00000440410.5:c.921A>T	ENSP00000417016.1:p.Glu307Asp
NM_000108.4:c.990A>T	NP_000099.2:p.Glu330Asp
NM_001289750.1:c.693A>T	NP_001276679.1:p.Glu231Asp
NM_001289751.1:c.921A>T	NP_001276680.1:p.Glu307Asp
NM_001289752.1:c.846A>T	NP_001276681.1:p.Glu282Asp
NM_000108.5:c.990A>T MANE Select	NP_000099.2:p.Glu330Asp