Canonical Allele Identifier: CA457108790

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107556028T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915583T>C , CM000669.2:g.107915583T>C	GRCh38
NC_000007.13:g.107556028T>C , CM000669.1:g.107556028T>C	GRCh37
NC_000007.12:g.107343264T>C	NCBI36
NG_008045.1:g.29443T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.762T>C MANE Select	ENSP00000205402.3:p.Asp254=
ENST00000205402.9:c.762T>C	ENSP00000205402.3:p.Asp254=
ENST00000415325.5:c.*436T>C	ENSP00000402593.1:n.*436T>C
ENST00000417551.5:c.762T>C	ENSP00000390667.1:p.Asp254=
ENST00000437604.6:c.618T>C	ENSP00000387542.2:p.Asp206=
ENST00000440410.5:c.693T>C	ENSP00000417016.1:p.Asp231=
ENST00000451081.5:c.*505T>C	ENSP00000388077.1:n.*505T>C
NM_000108.4:c.762T>C	NP_000099.2:p.Asp254=
NM_001289750.1:c.465T>C	NP_001276679.1:p.Asp155=
NM_001289751.1:c.693T>C	NP_001276680.1:p.Asp231=
NM_001289752.1:c.618T>C	NP_001276681.1:p.Asp206=
NM_000108.5:c.762T>C MANE Select	NP_000099.2:p.Asp254=