Canonical Allele Identifier: CA164258551

Gene: DLD

Linked Data

• dbSNP Id: rs886068228
• MyVariant Identifiers: chr7:g.107558072_107558073del (hg19) ; chr7:g.107917627_107917628del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917628_107917629del , CM000669.2:g.107917628_107917629del	GRCh38
NC_000007.13:g.107558073_107558074del , CM000669.1:g.107558073_107558074del	GRCh37
NC_000007.12:g.107345309_107345310del	NCBI36
NG_008045.1:g.31488_31489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1236+166_1236+167del MANE Select	ENSP00000205402.3:n.1236+166_1236+167del
ENST00000205402.9:c.1236+166_1236+167del	ENSP00000205402.3:n.1236+166_1236+167del
ENST00000415325.5:c.*910+166_*910+167del	ENSP00000402593.1:n.*910+166_*910+167del
ENST00000417551.5:c.1236+166_1236+167del	ENSP00000390667.1:n.1236+166_1236+167del
ENST00000437604.6:c.1092+166_1092+167del	ENSP00000387542.2:n.1092+166_1092+167del
ENST00000440410.5:c.1167+166_1167+167del	ENSP00000417016.1:n.1167+166_1167+167del
NM_000108.4:c.1236+166_1236+167del	NP_000099.2:n.1236+166_1236+167del
NM_001289750.1:c.939+166_939+167del	NP_001276679.1:n.939+166_939+167del
NM_001289751.1:c.1167+166_1167+167del	NP_001276680.1:n.1167+166_1167+167del
NM_001289752.1:c.1092+166_1092+167del	NP_001276681.1:n.1092+166_1092+167del
NM_000108.5:c.1236+166_1236+167del MANE Select	NP_000099.2:n.1236+166_1236+167del