Canonical Allele Identifier: CA963769

Gene: DPYD

Linked Data

• dbSNP Id: rs371587702
• ExAC: 1:98293709 G / C
• gnomAD v2: 1-98293709-G-C
• gnomAD v4: 1-97828153-G-C
• MyVariant Identifiers: chr1:g.98293709G>C (hg19) ; chr1:g.97828153G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828153G>C , CM000663.2:g.97828153G>C	GRCh38
NC_000001.10:g.98293709G>C , CM000663.1:g.98293709G>C	GRCh37
NC_000001.9:g.98066297G>C	NCBI36
NG_008807.2:g.97907C>G , LRG_722:g.97907C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.194C>G MANE Select	ENSP00000359211.3:p.Thr65Arg
ENST00000306031.5:c.194C>G	ENSP00000307107.5:p.Thr65Arg
ENST00000370192.7:c.194C>G	ENSP00000359211.3:p.Thr65Arg
NM_000110.3:c.194C>G , LRG_722t1:c.194C>G	NP_000101.2:p.Thr65Arg
NM_001160301.1:c.194C>G , LRG_722t2:c.194C>G	NP_001153773.1:p.Thr65Arg
XM_005270562.3:c.194C>G	XP_005270619.2:p.Thr65Arg
XM_006710397.2:c.194C>G	XP_006710460.1:p.Thr65Arg
XM_006710397.3:c.194C>G	XP_006710460.1:p.Thr65Arg
XM_017000507.1:c.83C>G	XP_016855996.1:p.Thr28Arg
XM_017000508.2:c.-517C>G	XP_016855997.1:n.-517C>G
XM_017000509.2:c.-415C>G	XP_016855998.1:n.-415C>G
XM_017000510.1:c.-415C>G	XP_016855999.1:n.-415C>G
XR_001737014.1:n.331C>G
NM_000110.4:c.194C>G MANE Select	NP_000101.2:p.Thr65Arg