Canonical Allele Identifier: CA740770745

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs1210430400
• gnomAD v3: 1-97305183-A-C
• gnomAD v4: 1-97305183-A-C
• MyVariant Identifiers: chr1:g.97770739A>C (hg19) ; chr1:g.97305183A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305183A>C , CM000663.2:g.97305183A>C	GRCh38
NC_000001.10:g.97770739A>C , CM000663.1:g.97770739A>C	GRCh37
NC_000001.9:g.97543327A>C	NCBI36
NG_008807.2:g.620877T>G , LRG_722:g.620877T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.2299+76T>G (DPYD) MANE Select	ENSP00000359211.3:n.2299+76T>G
ENST00000370192.7:c.2299+76T>G (DPYD)	ENSP00000359211.3:n.2299+76T>G
NM_000110.3:c.2299+76T>G , LRG_722t1:c.2299+76T>G (DPYD)	NP_000101.2:n.2299+76T>G
NR_046590.1:n.129-1006A>C (DPYD-AS1)
XM_005270562.3:c.2083+76T>G (DPYD)	XP_005270619.2:n.2083+76T>G
XM_006710397.2:c.2299+76T>G (DPYD)	XP_006710460.1:n.2299+76T>G
XM_006710397.3:c.2299+76T>G (DPYD)	XP_006710460.1:n.2299+76T>G
XM_017000507.1:c.2188+76T>G (DPYD)	XP_016855996.1:n.2188+76T>G
XM_017000508.2:c.1804+76T>G (DPYD)	XP_016855997.1:n.1804+76T>G
XM_017000509.2:c.1804+76T>G (DPYD)	XP_016855998.1:n.1804+76T>G
XM_017000510.1:c.1804+76T>G (DPYD)	XP_016855999.1:n.1804+76T>G
NM_000110.4:c.2299+76T>G (DPYD) MANE Select	NP_000101.2:n.2299+76T>G