Canonical Allele Identifier: CA4434729

Gene: DLD

Linked Data

• dbSNP Id: rs769068671
• ExAC: 7:107559616 A / T
• gnomAD v2: 7-107559616-A-T
• MyVariant Identifiers: chr7:g.107559616A>T (hg19) ; chr7:g.107919171A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919171A>T , CM000669.2:g.107919171A>T	GRCh38
NC_000007.13:g.107559616A>T , CM000669.1:g.107559616A>T	GRCh37
NC_000007.12:g.107346852A>T	NCBI36
NG_008045.1:g.33031A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1465-23A>T MANE Select	ENSP00000205402.3:n.1465-23A>T
ENST00000205402.9:c.1465-23A>T	ENSP00000205402.3:n.1465-23A>T
ENST00000415325.5:c.*1139-23A>T	ENSP00000402593.1:n.*1139-23A>T
ENST00000417551.5:c.1465-23A>T	ENSP00000390667.1:n.1465-23A>T
ENST00000437604.6:c.1321-23A>T	ENSP00000387542.2:n.1321-23A>T
ENST00000440410.5:c.1396-23A>T	ENSP00000417016.1:n.1396-23A>T
NM_000108.4:c.1465-23A>T	NP_000099.2:n.1465-23A>T
NM_001289750.1:c.1168-23A>T	NP_001276679.1:n.1168-23A>T
NM_001289751.1:c.1396-23A>T	NP_001276680.1:n.1396-23A>T
NM_001289752.1:c.1321-23A>T	NP_001276681.1:n.1321-23A>T
NM_000108.5:c.1465-23A>T MANE Select	NP_000099.2:n.1465-23A>T