Canonical Allele Identifier: CA368858461

Gene: DLD

Linked Data

• gnomAD v4: 7-107917406-T-G
• MyVariant Identifiers: chr7:g.107557851T>G (hg19) ; chr7:g.107917406T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917406T>G , CM000669.2:g.107917406T>G	GRCh38
NC_000007.13:g.107557851T>G , CM000669.1:g.107557851T>G	GRCh37
NC_000007.12:g.107345087T>G	NCBI36
NG_008045.1:g.31266T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1180T>G MANE Select	ENSP00000205402.3:p.Tyr394Asp
ENST00000205402.9:c.1180T>G	ENSP00000205402.3:p.Tyr394Asp
ENST00000415325.5:c.*854T>G	ENSP00000402593.1:n.*854T>G
ENST00000417551.5:c.1180T>G	ENSP00000390667.1:p.Tyr394Asp
ENST00000437604.6:c.1036T>G	ENSP00000387542.2:p.Tyr346Asp
ENST00000440410.5:c.1111T>G	ENSP00000417016.1:p.Tyr371Asp
NM_000108.4:c.1180T>G	NP_000099.2:p.Tyr394Asp
NM_001289750.1:c.883T>G	NP_001276679.1:p.Tyr295Asp
NM_001289751.1:c.1111T>G	NP_001276680.1:p.Tyr371Asp
NM_001289752.1:c.1036T>G	NP_001276681.1:p.Tyr346Asp
NM_000108.5:c.1180T>G MANE Select	NP_000099.2:p.Tyr394Asp