Canonical Allele Identifier: CA2696577537

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs2101037019

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305393T>C , CM000663.2:g.97305393T>C	GRCh38
NC_000001.10:g.97770949T>C , CM000663.1:g.97770949T>C	GRCh37
NC_000001.9:g.97543537T>C	NCBI36
NG_008807.2:g.620667A>G , LRG_722:g.620667A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2180-15A>G (DPYD) MANE Select	ENSP00000359211.3:n.2180-15A>G
ENST00000370192.7:c.2180-15A>G (DPYD)	ENSP00000359211.3:n.2180-15A>G
NM_000110.3:c.2180-15A>G , LRG_722t1:c.2180-15A>G (DPYD)	NP_000101.2:n.2180-15A>G
NR_046590.1:n.129-796T>C (DPYD-AS1)
XM_005270562.3:c.1964-15A>G (DPYD)	XP_005270619.2:n.1964-15A>G
XM_006710397.2:c.2180-15A>G (DPYD)	XP_006710460.1:n.2180-15A>G
XM_006710397.3:c.2180-15A>G (DPYD)	XP_006710460.1:n.2180-15A>G
XM_017000507.1:c.2069-15A>G (DPYD)	XP_016855996.1:n.2069-15A>G
XM_017000508.2:c.1685-15A>G (DPYD)	XP_016855997.1:n.1685-15A>G
XM_017000509.2:c.1685-15A>G (DPYD)	XP_016855998.1:n.1685-15A>G
XM_017000510.1:c.1685-15A>G (DPYD)	XP_016855999.1:n.1685-15A>G
NM_000110.4:c.2180-15A>G (DPYD) MANE Select	NP_000101.2:n.2180-15A>G