Canonical Allele Identifier: CA341375225

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1214674904
• gnomAD v2: 1-97770923-C-T
• gnomAD v4: 1-97305367-C-T
• MyVariant Identifiers: chr1:g.97770923C>T (hg19) ; chr1:g.97305367C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305367C>T , CM000663.2:g.97305367C>T	GRCh38
NC_000001.10:g.97770923C>T , CM000663.1:g.97770923C>T	GRCh37
NC_000001.9:g.97543511C>T	NCBI36
NG_008807.2:g.620693G>A , LRG_722:g.620693G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2191G>A (DPYD) MANE Select	ENSP00000359211.3:p.Gly731Ser
ENST00000370192.7:c.2191G>A (DPYD)	ENSP00000359211.3:p.Gly731Ser
NM_000110.3:c.2191G>A , LRG_722t1:c.2191G>A (DPYD)	NP_000101.2:p.Gly731Ser
NR_046590.1:n.129-822C>T (DPYD-AS1)
XM_005270562.3:c.1975G>A (DPYD)	XP_005270619.2:p.Gly659Ser
XM_006710397.2:c.2191G>A (DPYD)	XP_006710460.1:p.Gly731Ser
XM_006710397.3:c.2191G>A (DPYD)	XP_006710460.1:p.Gly731Ser
XM_017000507.1:c.2080G>A (DPYD)	XP_016855996.1:p.Gly694Ser
XM_017000508.2:c.1696G>A (DPYD)	XP_016855997.1:p.Gly566Ser
XM_017000509.2:c.1696G>A (DPYD)	XP_016855998.1:p.Gly566Ser
XM_017000510.1:c.1696G>A (DPYD)	XP_016855999.1:p.Gly566Ser
NM_000110.4:c.2191G>A (DPYD) MANE Select	NP_000101.2:p.Gly731Ser