Canonical Allele Identifier: CA16041121

Gene: DLD

Linked Data

• ClinVar Variation Id: 370700
• ClinVar RCV Id: RCV000411685 ; RCV004529563
• dbSNP Id: rs1057516698
• MyVariant Identifiers: chr7:g.107533717C>T (hg19) ; chr7:g.107893272C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893272C>T , CM000669.2:g.107893272C>T	GRCh38
NC_000007.13:g.107533717C>T , CM000669.1:g.107533717C>T	GRCh37
NC_000007.12:g.107320953C>T	NCBI36
NG_008045.1:g.7132C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.112C>T MANE Select	ENSP00000205402.3:p.Gln38Ter
ENST00000639772.1:c.112C>T	ENSP00000492159.1:p.Gln38Ter
ENST00000205402.9:c.112C>T	ENSP00000205402.3:p.Gln38Ter
ENST00000415325.5:c.112C>T	ENSP00000402593.1:p.Gln38Ter
ENST00000417551.5:c.112C>T	ENSP00000390667.1:p.Gln38Ter
ENST00000437604.6:c.112C>T	ENSP00000387542.2:p.Gln38Ter
ENST00000440410.5:c.112C>T	ENSP00000417016.1:p.Gln38Ter
ENST00000450038.5:c.112C>T	ENSP00000409590.1:p.Gln38Ter
ENST00000451081.5:c.112C>T	ENSP00000388077.1:p.Gln38Ter
ENST00000453354.5:n.177C>T
ENST00000460577.5:n.146C>T
ENST00000485066.1:n.201C>T
ENST00000494441.1:n.257C>T
NM_000108.4:c.112C>T	NP_000099.2:p.Gln38Ter
NM_001289750.1:c.-37C>T	NP_001276679.1:n.-37C>T
NM_001289751.1:c.112C>T	NP_001276680.1:p.Gln38Ter
NM_001289752.1:c.112C>T	NP_001276681.1:p.Gln38Ter
NM_000108.5:c.112C>T MANE Select	NP_000099.2:p.Gln38Ter