Canonical Allele Identifier: CA419140957

Gene: DPYD

Linked Data

• gnomAD v4: 1-97382456-C-A
• MyVariant Identifiers: chr1:g.97848012C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382456C>A , CM000663.2:g.97382456C>A	GRCh38
NC_000001.10:g.97848012C>A , CM000663.1:g.97848012C>A	GRCh37
NC_000001.9:g.97620600C>A	NCBI36
NG_008807.2:g.543604G>T , LRG_722:g.543604G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1911G>T MANE Select	ENSP00000359211.3:p.Val637=
ENST00000370192.7:c.1911G>T	ENSP00000359211.3:p.Val637=
NM_000110.3:c.1911G>T , LRG_722t1:c.1911G>T	NP_000101.2:p.Val637=
XM_005270562.3:c.1695G>T	XP_005270619.2:p.Val565=
XM_006710397.2:c.1911G>T	XP_006710460.1:p.Val637=
XR_947619.1:n.1347-1178C>A
XR_947620.1:n.1125-1178C>A
XR_947621.1:n.1347-1178C>A
XM_006710397.3:c.1911G>T	XP_006710460.1:p.Val637=
XM_017000507.1:c.1800G>T	XP_016855996.1:p.Val600=
XM_017000508.2:c.1416G>T	XP_016855997.1:p.Val472=
XM_017000509.2:c.1416G>T	XP_016855998.1:p.Val472=
XM_017000510.1:c.1416G>T	XP_016855999.1:p.Val472=
XR_001737686.2:n.692-1178C>A
XR_001737687.1:n.692-1178C>A
XR_001737688.2:n.692-1178C>A
NM_000110.4:c.1911G>T MANE Select	NP_000101.2:p.Val637=