Canonical Allele Identifier: CA457109806

Gene: DLD

Linked Data

• dbSNP Id: rs34453495
• gnomAD v2: 7-107559502-A-T
• gnomAD v4: 7-107919057-A-T
• MyVariant Identifiers: chr7:g.107559502A>T (hg19) ; chr7:g.107919057A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919057A>T , CM000669.2:g.107919057A>T	GRCh38
NC_000007.13:g.107559502A>T , CM000669.1:g.107559502A>T	GRCh37
NC_000007.12:g.107346738A>T	NCBI36
NG_008045.1:g.32917A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1422A>T MANE Select	ENSP00000205402.3:p.Gly474=
ENST00000205402.9:c.1422A>T	ENSP00000205402.3:p.Gly474=
ENST00000415325.5:c.*1096A>T	ENSP00000402593.1:n.*1096A>T
ENST00000417551.5:c.1422A>T	ENSP00000390667.1:p.Gly474=
ENST00000437604.6:c.1278A>T	ENSP00000387542.2:p.Gly426=
ENST00000440410.5:c.1353A>T	ENSP00000417016.1:p.Gly451=
NM_000108.4:c.1422A>T	NP_000099.2:p.Gly474=
NM_001289750.1:c.1125A>T	NP_001276679.1:p.Gly375=
NM_001289751.1:c.1353A>T	NP_001276680.1:p.Gly451=
NM_001289752.1:c.1278A>T	NP_001276681.1:p.Gly426=
NM_000108.5:c.1422A>T MANE Select	NP_000099.2:p.Gly474=