Canonical Allele Identifier: CA341376044

Gene: DPYD

Linked Data

• dbSNP Id: rs1245407981
• gnomAD v2: 1-97915679-C-T
• gnomAD v4: 1-97450123-C-T
• MyVariant Identifiers: chr1:g.97915679C>T (hg19) ; chr1:g.97450123C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450123C>T , CM000663.2:g.97450123C>T	GRCh38
NC_000001.10:g.97915679C>T , CM000663.1:g.97915679C>T	GRCh37
NC_000001.9:g.97688267C>T	NCBI36
NG_008807.2:g.475937G>A , LRG_722:g.475937G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1841G>A MANE Select	ENSP00000359211.3:p.Ser614Asn
ENST00000370192.7:c.1841G>A	ENSP00000359211.3:p.Ser614Asn
NM_000110.3:c.1841G>A , LRG_722t1:c.1841G>A	NP_000101.2:p.Ser614Asn
XM_005270562.3:c.1625G>A	XP_005270619.2:p.Ser542Asn
XM_006710397.2:c.1841G>A	XP_006710460.1:p.Ser614Asn
XM_006710397.3:c.1841G>A	XP_006710460.1:p.Ser614Asn
XM_017000507.1:c.1730G>A	XP_016855996.1:p.Ser577Asn
XM_017000508.2:c.1346G>A	XP_016855997.1:p.Ser449Asn
XM_017000509.2:c.1346G>A	XP_016855998.1:p.Ser449Asn
XM_017000510.1:c.1346G>A	XP_016855999.1:p.Ser449Asn
NM_000110.4:c.1841G>A MANE Select	NP_000101.2:p.Ser614Asn