Canonical Allele Identifier: CA368856711

Gene: DLD

Linked Data

• gnomAD v4: 7-107915507-G-T
• MyVariant Identifiers: chr7:g.107555952G>T (hg19) ; chr7:g.107915507G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915507G>T , CM000669.2:g.107915507G>T	GRCh38
NC_000007.13:g.107555952G>T , CM000669.1:g.107555952G>T	GRCh37
NC_000007.12:g.107343188G>T	NCBI36
NG_008045.1:g.29367G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.686G>T MANE Select	ENSP00000205402.3:p.Gly229Val
ENST00000205402.9:c.686G>T	ENSP00000205402.3:p.Gly229Val
ENST00000415325.5:c.*360G>T	ENSP00000402593.1:n.*360G>T
ENST00000417551.5:c.686G>T	ENSP00000390667.1:p.Gly229Val
ENST00000437604.6:c.542G>T	ENSP00000387542.2:p.Gly181Val
ENST00000440410.5:c.617G>T	ENSP00000417016.1:p.Gly206Val
ENST00000451081.5:c.*429G>T	ENSP00000388077.1:n.*429G>T
NM_000108.4:c.686G>T	NP_000099.2:p.Gly229Val
NM_001289750.1:c.389G>T	NP_001276679.1:p.Gly130Val
NM_001289751.1:c.617G>T	NP_001276680.1:p.Gly206Val
NM_001289752.1:c.542G>T	NP_001276681.1:p.Gly181Val
NM_000108.5:c.686G>T MANE Select	NP_000099.2:p.Gly229Val