Canonical Allele Identifier: CA341375839

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97847997C>T (hg19) ; chr1:g.97382441C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382441C>T , CM000663.2:g.97382441C>T	GRCh38
NC_000001.10:g.97847997C>T , CM000663.1:g.97847997C>T	GRCh37
NC_000001.9:g.97620585C>T	NCBI36
NG_008807.2:g.543619G>A , LRG_722:g.543619G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1926G>A MANE Select	ENSP00000359211.3:p.Met642Ile
ENST00000370192.7:c.1926G>A	ENSP00000359211.3:p.Met642Ile
NM_000110.3:c.1926G>A , LRG_722t1:c.1926G>A	NP_000101.2:p.Met642Ile
XM_005270562.3:c.1710G>A	XP_005270619.2:p.Met570Ile
XM_006710397.2:c.1926G>A	XP_006710460.1:p.Met642Ile
XR_947619.1:n.1347-1193C>T
XR_947620.1:n.1125-1193C>T
XR_947621.1:n.1347-1193C>T
XM_006710397.3:c.1926G>A	XP_006710460.1:p.Met642Ile
XM_017000507.1:c.1815G>A	XP_016855996.1:p.Met605Ile
XM_017000508.2:c.1431G>A	XP_016855997.1:p.Met477Ile
XM_017000509.2:c.1431G>A	XP_016855998.1:p.Met477Ile
XM_017000510.1:c.1431G>A	XP_016855999.1:p.Met477Ile
XR_001737686.2:n.692-1193C>T
XR_001737687.1:n.692-1193C>T
XR_001737688.2:n.692-1193C>T
NM_000110.4:c.1926G>A MANE Select	NP_000101.2:p.Met642Ile