Canonical Allele Identifier: CA368858008

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557722T>G (hg19) ; chr7:g.107917277T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917277T>G , CM000669.2:g.107917277T>G	GRCh38
NC_000007.13:g.107557722T>G , CM000669.1:g.107557722T>G	GRCh37
NC_000007.12:g.107344958T>G	NCBI36
NG_008045.1:g.31137T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1051T>G MANE Select	ENSP00000205402.3:p.Tyr351Asp
ENST00000205402.9:c.1051T>G	ENSP00000205402.3:p.Tyr351Asp
ENST00000415325.5:c.*725T>G	ENSP00000402593.1:n.*725T>G
ENST00000417551.5:c.1051T>G	ENSP00000390667.1:p.Tyr351Asp
ENST00000437604.6:c.907T>G	ENSP00000387542.2:p.Tyr303Asp
ENST00000440410.5:c.982T>G	ENSP00000417016.1:p.Tyr328Asp
NM_000108.4:c.1051T>G	NP_000099.2:p.Tyr351Asp
NM_001289750.1:c.754T>G	NP_001276679.1:p.Tyr252Asp
NM_001289751.1:c.982T>G	NP_001276680.1:p.Tyr328Asp
NM_001289752.1:c.907T>G	NP_001276681.1:p.Tyr303Asp
NM_000108.5:c.1051T>G MANE Select	NP_000099.2:p.Tyr351Asp