Canonical Allele Identifier: CA27460769

Gene: DPYD DPYD-AS1

Linked Data

• dbSNP Id: rs765256175
• gnomAD v2: 1-97564394-A-G
• gnomAD v3: 1-97098838-A-G
• gnomAD v4: 1-97098838-A-G
• MyVariant Identifiers: chr1:g.97564394A>G (hg19) ; chr1:g.97098838A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97098838A>G , CM000663.2:g.97098838A>G	GRCh38
NC_000001.10:g.97564394A>G , CM000663.1:g.97564394A>G	GRCh37
NC_000001.9:g.97336982A>G	NCBI36
NG_008807.2:g.827222T>C , LRG_722:g.827222T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2623-206T>C (DPYD) MANE Select	ENSP00000359211.3:n.2623-206T>C
ENST00000370192.7:c.2623-206T>C (DPYD)	ENSP00000359211.3:n.2623-206T>C
NM_000110.3:c.2623-206T>C , LRG_722t1:c.2623-206T>C (DPYD)	NP_000101.2:n.2623-206T>C
NR_046590.1:n.64+2852A>G (DPYD-AS1)
XM_005270562.3:c.2407-206T>C (DPYD)	XP_005270619.2:n.2407-206T>C
XM_017000507.1:c.2512-206T>C (DPYD)	XP_016855996.1:n.2512-206T>C
XM_017000508.2:c.2128-206T>C (DPYD)	XP_016855997.1:n.2128-206T>C
XM_017000509.2:c.2128-206T>C (DPYD)	XP_016855998.1:n.2128-206T>C
XM_017000510.1:c.2128-206T>C (DPYD)	XP_016855999.1:n.2128-206T>C
NM_000110.4:c.2623-206T>C (DPYD) MANE Select	NP_000101.2:n.2623-206T>C