Canonical Allele Identifier: CA4434348

Gene: DLD

Linked Data

• dbSNP Id: rs761108284
• ExAC: 7:107533692 A / T
• gnomAD v2: 7-107533692-A-T
• gnomAD v3: 7-107893247-A-T
• gnomAD v4: 7-107893247-A-T
• MyVariant Identifiers: chr7:g.107533692A>T (hg19) ; chr7:g.107893247A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893247A>T , CM000669.2:g.107893247A>T	GRCh38
NC_000007.13:g.107533692A>T , CM000669.1:g.107533692A>T	GRCh37
NC_000007.12:g.107320928A>T	NCBI36
NG_008045.1:g.7107A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.87A>T MANE Select	ENSP00000205402.3:p.Ala29=
ENST00000639772.1:c.87A>T	ENSP00000492159.1:p.Ala29=
ENST00000205402.9:c.87A>T	ENSP00000205402.3:p.Ala29=
ENST00000415325.5:c.87A>T	ENSP00000402593.1:p.Ala29=
ENST00000417551.5:c.87A>T	ENSP00000390667.1:p.Ala29=
ENST00000437604.6:c.87A>T	ENSP00000387542.2:p.Ala29=
ENST00000440410.5:c.87A>T	ENSP00000417016.1:p.Ala29=
ENST00000450038.5:c.87A>T	ENSP00000409590.1:p.Ala29=
ENST00000451081.5:c.87A>T	ENSP00000388077.1:p.Ala29=
ENST00000453354.5:n.152A>T
ENST00000460577.5:n.121A>T
ENST00000485066.1:n.176A>T
ENST00000494441.1:n.232A>T
NM_000108.4:c.87A>T	NP_000099.2:p.Ala29=
NM_001289750.1:c.-62A>T	NP_001276679.1:n.-62A>T
NM_001289751.1:c.87A>T	NP_001276680.1:p.Ala29=
NM_001289752.1:c.87A>T	NP_001276681.1:p.Ala29=
NM_000108.5:c.87A>T MANE Select	NP_000099.2:p.Ala29=