Canonical Allele Identifier: CA341377562

Gene: DPYD

Linked Data

• dbSNP Id: rs1651162700
• gnomAD v3: 1-97549615-A-C
• gnomAD v4: 1-97549615-A-C
• MyVariant Identifiers: chr1:g.98015171A>C (hg19) ; chr1:g.97549615A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549615A>C , CM000663.2:g.97549615A>C	GRCh38
NC_000001.10:g.98015171A>C , CM000663.1:g.98015171A>C	GRCh37
NC_000001.9:g.97787759A>C	NCBI36
NG_008807.2:g.376445T>G , LRG_722:g.376445T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1469T>G MANE Select	ENSP00000359211.3:p.Val490Gly
ENST00000370192.7:c.1469T>G	ENSP00000359211.3:p.Val490Gly
NM_000110.3:c.1469T>G , LRG_722t1:c.1469T>G	NP_000101.2:p.Val490Gly
XM_005270562.3:c.1469T>G	XP_005270619.2:p.Val490Gly
XM_006710397.2:c.1469T>G	XP_006710460.1:p.Val490Gly
XM_006710397.3:c.1469T>G	XP_006710460.1:p.Val490Gly
XM_017000507.1:c.1358T>G	XP_016855996.1:p.Val453Gly
XM_017000508.2:c.974T>G	XP_016855997.1:p.Val325Gly
XM_017000509.2:c.974T>G	XP_016855998.1:p.Val325Gly
XM_017000510.1:c.974T>G	XP_016855999.1:p.Val325Gly
NM_000110.4:c.1469T>G MANE Select	NP_000101.2:p.Val490Gly