Canonical Allele Identifier: CA457109380

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557751A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917306A>C , CM000669.2:g.107917306A>C	GRCh38
NC_000007.13:g.107557751A>C , CM000669.1:g.107557751A>C	GRCh37
NC_000007.12:g.107344987A>C	NCBI36
NG_008045.1:g.31166A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1080A>C MANE Select	ENSP00000205402.3:p.Pro360=
ENST00000205402.9:c.1080A>C	ENSP00000205402.3:p.Pro360=
ENST00000415325.5:c.*754A>C	ENSP00000402593.1:n.*754A>C
ENST00000417551.5:c.1080A>C	ENSP00000390667.1:p.Pro360=
ENST00000437604.6:c.936A>C	ENSP00000387542.2:p.Pro312=
ENST00000440410.5:c.1011A>C	ENSP00000417016.1:p.Pro337=
NM_000108.4:c.1080A>C	NP_000099.2:p.Pro360=
NM_001289750.1:c.783A>C	NP_001276679.1:p.Pro261=
NM_001289751.1:c.1011A>C	NP_001276680.1:p.Pro337=
NM_001289752.1:c.936A>C	NP_001276681.1:p.Pro312=
NM_000108.5:c.1080A>C MANE Select	NP_000099.2:p.Pro360=