Canonical Allele Identifier: CA2646704965

Gene: DPYD

Linked Data

• gnomAD v4: 1-97373492-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97373492A>G , CM000663.2:g.97373492A>G	GRCh38
NC_000001.10:g.97839048A>G , CM000663.1:g.97839048A>G	GRCh37
NC_000001.9:g.97611636A>G	NCBI36
NG_008807.2:g.552568T>C , LRG_722:g.552568T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2058+69T>C MANE Select	ENSP00000359211.3:n.2058+69T>C
ENST00000370192.7:c.2058+69T>C	ENSP00000359211.3:n.2058+69T>C
NM_000110.3:c.2058+69T>C , LRG_722t1:c.2058+69T>C	NP_000101.2:n.2058+69T>C
XM_005270562.3:c.1842+69T>C	XP_005270619.2:n.1842+69T>C
XM_006710397.2:c.2058+69T>C	XP_006710460.1:n.2058+69T>C
XR_947619.1:n.1125-2036A>G
XR_947620.1:n.1124+6291A>G
XR_947621.1:n.1125-2036A>G
XM_006710397.3:c.2058+69T>C	XP_006710460.1:n.2058+69T>C
XM_017000507.1:c.1947+69T>C	XP_016855996.1:n.1947+69T>C
XM_017000508.2:c.1563+69T>C	XP_016855997.1:n.1563+69T>C
XM_017000509.2:c.1563+69T>C	XP_016855998.1:n.1563+69T>C
XM_017000510.1:c.1563+69T>C	XP_016855999.1:n.1563+69T>C
NM_000110.4:c.2058+69T>C MANE Select	NP_000101.2:n.2058+69T>C