Canonical Allele Identifier: CA368859638

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107559666A>T (hg19) ; chr7:g.107919221A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919221A>T , CM000669.2:g.107919221A>T	GRCh38
NC_000007.13:g.107559666A>T , CM000669.1:g.107559666A>T	GRCh37
NC_000007.12:g.107346902A>T	NCBI36
NG_008045.1:g.33081A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1492A>T MANE Select	ENSP00000205402.3:p.Asn498Tyr
ENST00000205402.9:c.1492A>T	ENSP00000205402.3:p.Asn498Tyr
ENST00000415325.5:c.*1166A>T	ENSP00000402593.1:n.*1166A>T
ENST00000417551.5:c.1492A>T	ENSP00000390667.1:p.Asn498Tyr
ENST00000437604.6:c.1348A>T	ENSP00000387542.2:p.Asn450Tyr
ENST00000440410.5:c.1423A>T	ENSP00000417016.1:p.Asn475Tyr
NM_000108.4:c.1492A>T	NP_000099.2:p.Asn498Tyr
NM_001289750.1:c.1195A>T	NP_001276679.1:p.Asn399Tyr
NM_001289751.1:c.1423A>T	NP_001276680.1:p.Asn475Tyr
NM_001289752.1:c.1348A>T	NP_001276681.1:p.Asn450Tyr
NM_000108.5:c.1492A>T MANE Select	NP_000099.2:p.Asn498Tyr