Canonical Allele Identifier: CA341375763

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97847966G>A (hg19) ; chr1:g.97382410G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382410G>A , CM000663.2:g.97382410G>A	GRCh38
NC_000001.10:g.97847966G>A , CM000663.1:g.97847966G>A	GRCh37
NC_000001.9:g.97620554G>A	NCBI36
NG_008807.2:g.543650C>T , LRG_722:g.543650C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1957C>T MANE Select	ENSP00000359211.3:p.Leu653Phe
ENST00000370192.7:c.1957C>T	ENSP00000359211.3:p.Leu653Phe
NM_000110.3:c.1957C>T , LRG_722t1:c.1957C>T	NP_000101.2:p.Leu653Phe
XM_005270562.3:c.1741C>T	XP_005270619.2:p.Leu581Phe
XM_006710397.2:c.1957C>T	XP_006710460.1:p.Leu653Phe
XR_947619.1:n.1347-1224G>A
XR_947620.1:n.1125-1224G>A
XR_947621.1:n.1347-1224G>A
XM_006710397.3:c.1957C>T	XP_006710460.1:p.Leu653Phe
XM_017000507.1:c.1846C>T	XP_016855996.1:p.Leu616Phe
XM_017000508.2:c.1462C>T	XP_016855997.1:p.Leu488Phe
XM_017000509.2:c.1462C>T	XP_016855998.1:p.Leu488Phe
XM_017000510.1:c.1462C>T	XP_016855999.1:p.Leu488Phe
XR_001737686.2:n.692-1224G>A
XR_001737687.1:n.692-1224G>A
XR_001737688.2:n.692-1224G>A
NM_000110.4:c.1957C>T MANE Select	NP_000101.2:p.Leu653Phe