Canonical Allele Identifier: CA457106828

Gene: DLD

Linked Data

• ClinVar Variation Id: 1095111
• ClinVar RCV Id: RCV001415894
• dbSNP Id: rs2031632982
• gnomAD v4: 7-107893208-T-C
• MyVariant Identifiers: chr7:g.107533653T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893208T>C , CM000669.2:g.107893208T>C	GRCh38
NC_000007.13:g.107533653T>C , CM000669.1:g.107533653T>C	GRCh37
NC_000007.12:g.107320889T>C	NCBI36
NG_008045.1:g.7068T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.48T>C MANE Select	ENSP00000205402.3:p.His16=
ENST00000639772.1:c.48T>C	ENSP00000492159.1:p.His16=
ENST00000205402.9:c.48T>C	ENSP00000205402.3:p.His16=
ENST00000415325.5:c.48T>C	ENSP00000402593.1:p.His16=
ENST00000417551.5:c.48T>C	ENSP00000390667.1:p.His16=
ENST00000437604.6:c.48T>C	ENSP00000387542.2:p.His16=
ENST00000440410.5:c.48T>C	ENSP00000417016.1:p.His16=
ENST00000450038.5:c.48T>C	ENSP00000409590.1:p.His16=
ENST00000451081.5:c.48T>C	ENSP00000388077.1:p.His16=
ENST00000453354.5:n.113T>C
ENST00000460577.5:n.82T>C
ENST00000485066.1:n.137T>C
ENST00000494441.1:n.193T>C
NM_000108.4:c.48T>C	NP_000099.2:p.His16=
NM_001289750.1:c.-101T>C	NP_001276679.1:n.-101T>C
NM_001289751.1:c.48T>C	NP_001276680.1:p.His16=
NM_001289752.1:c.48T>C	NP_001276681.1:p.His16=
NM_000108.5:c.48T>C MANE Select	NP_000099.2:p.His16=