Canonical Allele Identifier: CA341379504

Gene: DPYD

Linked Data

• gnomAD v4: 1-97828177-T-C
• MyVariant Identifiers: chr1:g.98293733T>C (hg19) ; chr1:g.97828177T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97828177T>C , CM000663.2:g.97828177T>C	GRCh38
NC_000001.10:g.98293733T>C , CM000663.1:g.98293733T>C	GRCh37
NC_000001.9:g.98066321T>C	NCBI36
NG_008807.2:g.97883A>G , LRG_722:g.97883A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.170A>G MANE Select	ENSP00000359211.3:p.Asn57Ser
ENST00000306031.5:c.170A>G	ENSP00000307107.5:p.Asn57Ser
ENST00000370192.7:c.170A>G	ENSP00000359211.3:p.Asn57Ser
NM_000110.3:c.170A>G , LRG_722t1:c.170A>G	NP_000101.2:p.Asn57Ser
NM_001160301.1:c.170A>G , LRG_722t2:c.170A>G	NP_001153773.1:p.Asn57Ser
XM_005270562.3:c.170A>G	XP_005270619.2:p.Asn57Ser
XM_006710397.2:c.170A>G	XP_006710460.1:p.Asn57Ser
XM_006710397.3:c.170A>G	XP_006710460.1:p.Asn57Ser
XM_017000507.1:c.59A>G	XP_016855996.1:p.Asn20Ser
XM_017000508.2:c.-541A>G	XP_016855997.1:n.-541A>G
XM_017000509.2:c.-439A>G	XP_016855998.1:n.-439A>G
XM_017000510.1:c.-439A>G	XP_016855999.1:n.-439A>G
XR_001737014.1:n.307A>G
NM_000110.4:c.170A>G MANE Select	NP_000101.2:p.Asn57Ser