Canonical Allele Identifier: CA368852929

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107533654T>A (hg19) ; chr7:g.107893209T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893209T>A , CM000669.2:g.107893209T>A	GRCh38
NC_000007.13:g.107533654T>A , CM000669.1:g.107533654T>A	GRCh37
NC_000007.12:g.107320890T>A	NCBI36
NG_008045.1:g.7069T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.49T>A MANE Select	ENSP00000205402.3:p.Phe17Ile
ENST00000639772.1:c.49T>A	ENSP00000492159.1:p.Phe17Ile
ENST00000205402.9:c.49T>A	ENSP00000205402.3:p.Phe17Ile
ENST00000415325.5:c.49T>A	ENSP00000402593.1:p.Phe17Ile
ENST00000417551.5:c.49T>A	ENSP00000390667.1:p.Phe17Ile
ENST00000437604.6:c.49T>A	ENSP00000387542.2:p.Phe17Ile
ENST00000440410.5:c.49T>A	ENSP00000417016.1:p.Phe17Ile
ENST00000450038.5:c.49T>A	ENSP00000409590.1:p.Phe17Ile
ENST00000451081.5:c.49T>A	ENSP00000388077.1:p.Phe17Ile
ENST00000453354.5:n.114T>A
ENST00000460577.5:n.83T>A
ENST00000485066.1:n.138T>A
ENST00000494441.1:n.194T>A
NM_000108.4:c.49T>A	NP_000099.2:p.Phe17Ile
NM_001289750.1:c.-100T>A	NP_001276679.1:n.-100T>A
NM_001289751.1:c.49T>A	NP_001276680.1:p.Phe17Ile
NM_001289752.1:c.49T>A	NP_001276681.1:p.Phe17Ile
NM_000108.5:c.49T>A MANE Select	NP_000099.2:p.Phe17Ile