Canonical Allele Identifier: CA2838195956

Gene: DPYD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97533092T>G , CM000663.2:g.97533092T>G	GRCh38
NC_000001.10:g.97998648T>G , CM000663.1:g.97998648T>G	GRCh37
NC_000001.9:g.97771236T>G	NCBI36
NG_008807.2:g.392968A>C , LRG_722:g.392968A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1524+16468A>C MANE Select	ENSP00000359211.3:n.1524+16468A>C
ENST00000370192.7:c.1524+16468A>C	ENSP00000359211.3:n.1524+16468A>C
NM_000110.3:c.1524+16468A>C , LRG_722t1:c.1524+16468A>C	NP_000101.2:n.1524+16468A>C
XM_005270562.3:c.1524+16468A>C	XP_005270619.2:n.1524+16468A>C
XM_006710397.2:c.1524+16468A>C	XP_006710460.1:n.1524+16468A>C
XM_006710397.3:c.1524+16468A>C	XP_006710460.1:n.1524+16468A>C
XM_017000507.1:c.1413+16468A>C	XP_016855996.1:n.1413+16468A>C
XM_017000508.2:c.1029+16468A>C	XP_016855997.1:n.1029+16468A>C
XM_017000509.2:c.1029+16468A>C	XP_016855998.1:n.1029+16468A>C
XM_017000510.1:c.1029+16468A>C	XP_016855999.1:n.1029+16468A>C
NM_000110.4:c.1524+16468A>C MANE Select	NP_000101.2:n.1524+16468A>C