Canonical Allele Identifier: CA2646703674

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97192998-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97192998T>C , CM000663.2:g.97192998T>C	GRCh38
NC_000001.10:g.97658554T>C , CM000663.1:g.97658554T>C	GRCh37
NC_000001.9:g.97431142T>C	NCBI36
NG_008807.2:g.733062A>G , LRG_722:g.733062A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2622+71A>G (DPYD) MANE Select	ENSP00000359211.3:n.2622+71A>G
ENST00000370192.7:c.2622+71A>G (DPYD)	ENSP00000359211.3:n.2622+71A>G
NM_000110.3:c.2622+71A>G , LRG_722t1:c.2622+71A>G (DPYD)	NP_000101.2:n.2622+71A>G
NR_046590.1:n.65-72416T>C (DPYD-AS1)
XM_005270562.3:c.2406+71A>G (DPYD)	XP_005270619.2:n.2406+71A>G
XM_006710397.2:c.2623-23A>G (DPYD)	XP_006710460.1:n.2623-23A>G
XM_006710397.3:c.2623-23A>G (DPYD)	XP_006710460.1:n.2623-23A>G
XM_017000507.1:c.2511+71A>G (DPYD)	XP_016855996.1:n.2511+71A>G
XM_017000508.2:c.2127+71A>G (DPYD)	XP_016855997.1:n.2127+71A>G
XM_017000509.2:c.2127+71A>G (DPYD)	XP_016855998.1:n.2127+71A>G
XM_017000510.1:c.2127+71A>G (DPYD)	XP_016855999.1:n.2127+71A>G
NM_000110.4:c.2622+71A>G (DPYD) MANE Select	NP_000101.2:n.2622+71A>G