Canonical Allele Identifier: CA27744905

Gene: DPYD

Linked Data

• dbSNP Id: rs538711405
• gnomAD v3: 1-97883184-T-C
• gnomAD v4: 1-97883184-T-C
• MyVariant Identifiers: chr1:g.98348740T>C (hg19) ; chr1:g.97883184T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97883184T>C , CM000663.2:g.97883184T>C	GRCh38
NC_000001.10:g.98348740T>C , CM000663.1:g.98348740T>C	GRCh37
NC_000001.9:g.98121328T>C	NCBI36
NG_008807.2:g.42876A>G , LRG_722:g.42876A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.150+80A>G MANE Select	ENSP00000359211.3:n.150+80A>G
ENST00000306031.5:c.150+80A>G	ENSP00000307107.5:n.150+80A>G
ENST00000370192.7:c.150+80A>G	ENSP00000359211.3:n.150+80A>G
ENST00000460019.1:n.225+80A>G
NM_000110.3:c.150+80A>G , LRG_722t1:c.150+80A>G	NP_000101.2:n.150+80A>G
NM_001160301.1:c.150+80A>G , LRG_722t2:c.150+80A>G	NP_001153773.1:n.150+80A>G
XM_005270562.3:c.150+80A>G	XP_005270619.2:n.150+80A>G
XM_006710397.2:c.150+80A>G	XP_006710460.1:n.150+80A>G
XM_006710397.3:c.150+80A>G	XP_006710460.1:n.150+80A>G
XM_017000507.1:c.39+37700A>G	XP_016855996.1:n.39+37700A>G
XM_017000508.2:c.-561+80A>G	XP_016855997.1:n.-561+80A>G
XM_017000509.2:c.-459+80A>G	XP_016855998.1:n.-459+80A>G
XM_017000510.1:c.-459+37700A>G	XP_016855999.1:n.-459+37700A>G
XR_001737014.1:n.287+80A>G
NM_000110.4:c.150+80A>G MANE Select	NP_000101.2:n.150+80A>G