Canonical Allele Identifier: CA368858673

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557909T>C (hg19) ; chr7:g.107917464T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917464T>C , CM000669.2:g.107917464T>C	GRCh38
NC_000007.13:g.107557909T>C , CM000669.1:g.107557909T>C	GRCh37
NC_000007.12:g.107345145T>C	NCBI36
NG_008045.1:g.31324T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1236+2T>C MANE Select	ENSP00000205402.3:n.1236+2T>C
ENST00000205402.9:c.1236+2T>C	ENSP00000205402.3:n.1236+2T>C
ENST00000415325.5:c.*910+2T>C	ENSP00000402593.1:n.*910+2T>C
ENST00000417551.5:c.1236+2T>C	ENSP00000390667.1:n.1236+2T>C
ENST00000437604.6:c.1092+2T>C	ENSP00000387542.2:n.1092+2T>C
ENST00000440410.5:c.1167+2T>C	ENSP00000417016.1:n.1167+2T>C
NM_000108.4:c.1236+2T>C	NP_000099.2:n.1236+2T>C
NM_001289750.1:c.939+2T>C	NP_001276679.1:n.939+2T>C
NM_001289751.1:c.1167+2T>C	NP_001276680.1:n.1167+2T>C
NM_001289752.1:c.1092+2T>C	NP_001276681.1:n.1092+2T>C
NM_000108.5:c.1236+2T>C MANE Select	NP_000099.2:n.1236+2T>C