Canonical Allele Identifier: CA368858332

Gene: DLD

Linked Data

• dbSNP Id: rs1319018195
• gnomAD v2: 7-107557813-C-G
• MyVariant Identifiers: chr7:g.107557813C>G (hg19) ; chr7:g.107917368C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917368C>G , CM000669.2:g.107917368C>G	GRCh38
NC_000007.13:g.107557813C>G , CM000669.1:g.107557813C>G	GRCh37
NC_000007.12:g.107345049C>G	NCBI36
NG_008045.1:g.31228C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1142C>G MANE Select	ENSP00000205402.3:p.Ala381Gly
ENST00000205402.9:c.1142C>G	ENSP00000205402.3:p.Ala381Gly
ENST00000415325.5:c.*816C>G	ENSP00000402593.1:n.*816C>G
ENST00000417551.5:c.1142C>G	ENSP00000390667.1:p.Ala381Gly
ENST00000437604.6:c.998C>G	ENSP00000387542.2:p.Ala333Gly
ENST00000440410.5:c.1073C>G	ENSP00000417016.1:p.Ala358Gly
NM_000108.4:c.1142C>G	NP_000099.2:p.Ala381Gly
NM_001289750.1:c.845C>G	NP_001276679.1:p.Ala282Gly
NM_001289751.1:c.1073C>G	NP_001276680.1:p.Ala358Gly
NM_001289752.1:c.998C>G	NP_001276681.1:p.Ala333Gly
NM_000108.5:c.1142C>G MANE Select	NP_000099.2:p.Ala381Gly