Canonical Allele Identifier: CA457107087

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107533722G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893277G>T , CM000669.2:g.107893277G>T	GRCh38
NC_000007.13:g.107533722G>T , CM000669.1:g.107533722G>T	GRCh37
NC_000007.12:g.107320958G>T	NCBI36
NG_008045.1:g.7137G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.117G>T MANE Select	ENSP00000205402.3:p.Pro39=
ENST00000639772.1:c.117G>T	ENSP00000492159.1:p.Pro39=
ENST00000205402.9:c.117G>T	ENSP00000205402.3:p.Pro39=
ENST00000415325.5:c.117G>T	ENSP00000402593.1:p.Pro39=
ENST00000417551.5:c.117G>T	ENSP00000390667.1:p.Pro39=
ENST00000437604.6:c.117G>T	ENSP00000387542.2:p.Pro39=
ENST00000440410.5:c.117G>T	ENSP00000417016.1:p.Pro39=
ENST00000450038.5:c.117G>T	ENSP00000409590.1:p.Pro39=
ENST00000451081.5:c.117G>T	ENSP00000388077.1:p.Pro39=
ENST00000453354.5:n.182G>T
ENST00000460577.5:n.151G>T
ENST00000485066.1:n.206G>T
ENST00000494441.1:n.262G>T
NM_000108.4:c.117G>T	NP_000099.2:p.Pro39=
NM_001289750.1:c.-32G>T	NP_001276679.1:n.-32G>T
NM_001289751.1:c.117G>T	NP_001276680.1:p.Pro39=
NM_001289752.1:c.117G>T	NP_001276681.1:p.Pro39=
NM_000108.5:c.117G>T MANE Select	NP_000099.2:p.Pro39=