Canonical Allele Identifier: CA368856749

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107555964A>T (hg19) ; chr7:g.107915519A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915519A>T , CM000669.2:g.107915519A>T	GRCh38
NC_000007.13:g.107555964A>T , CM000669.1:g.107555964A>T	GRCh37
NC_000007.12:g.107343200A>T	NCBI36
NG_008045.1:g.29379A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.698A>T MANE Select	ENSP00000205402.3:p.Gln233Leu
ENST00000205402.9:c.698A>T	ENSP00000205402.3:p.Gln233Leu
ENST00000415325.5:c.*372A>T	ENSP00000402593.1:n.*372A>T
ENST00000417551.5:c.698A>T	ENSP00000390667.1:p.Gln233Leu
ENST00000437604.6:c.554A>T	ENSP00000387542.2:p.Gln185Leu
ENST00000440410.5:c.629A>T	ENSP00000417016.1:p.Gln210Leu
ENST00000451081.5:c.*441A>T	ENSP00000388077.1:n.*441A>T
NM_000108.4:c.698A>T	NP_000099.2:p.Gln233Leu
NM_001289750.1:c.401A>T	NP_001276679.1:p.Gln134Leu
NM_001289751.1:c.629A>T	NP_001276680.1:p.Gln210Leu
NM_001289752.1:c.554A>T	NP_001276681.1:p.Gln185Leu
NM_000108.5:c.698A>T MANE Select	NP_000099.2:p.Gln233Leu