Canonical Allele Identifier: CA740786258

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1294925803
• MyVariant Identifiers: chr1:g.97658860del (hg19) ; chr1:g.97193304del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97193306del , CM000663.2:g.97193306del	GRCh38
NC_000001.10:g.97658862del , CM000663.1:g.97658862del	GRCh37
NC_000001.9:g.97431450del	NCBI36
NG_008807.2:g.732756del , LRG_722:g.732756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2443-56del (DPYD) MANE Select	ENSP00000359211.3:n.2443-56del
ENST00000370192.7:c.2443-56del (DPYD)	ENSP00000359211.3:n.2443-56del
NM_000110.3:c.2443-56del , LRG_722t1:c.2443-56del (DPYD)	NP_000101.2:n.2443-56del
NR_046590.1:n.65-72108del (DPYD-AS1)
XM_005270562.3:c.2227-56del (DPYD)	XP_005270619.2:n.2227-56del
XM_006710397.2:c.2443-56del (DPYD)	XP_006710460.1:n.2443-56del
XM_006710397.3:c.2443-56del (DPYD)	XP_006710460.1:n.2443-56del
XM_017000507.1:c.2332-56del (DPYD)	XP_016855996.1:n.2332-56del
XM_017000508.2:c.1948-56del (DPYD)	XP_016855997.1:n.1948-56del
XM_017000509.2:c.1948-56del (DPYD)	XP_016855998.1:n.1948-56del
XM_017000510.1:c.1948-56del (DPYD)	XP_016855999.1:n.1948-56del
NM_000110.4:c.2443-56del (DPYD) MANE Select	NP_000101.2:n.2443-56del