Canonical Allele Identifier: CA341375743

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97847957T>A (hg19) ; chr1:g.97382401T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382401T>A , CM000663.2:g.97382401T>A	GRCh38
NC_000001.10:g.97847957T>A , CM000663.1:g.97847957T>A	GRCh37
NC_000001.9:g.97620545T>A	NCBI36
NG_008807.2:g.543659A>T , LRG_722:g.543659A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1966A>T MANE Select	ENSP00000359211.3:p.Lys656Ter
ENST00000370192.7:c.1966A>T	ENSP00000359211.3:p.Lys656Ter
NM_000110.3:c.1966A>T , LRG_722t1:c.1966A>T	NP_000101.2:p.Lys656Ter
XM_005270562.3:c.1750A>T	XP_005270619.2:p.Lys584Ter
XM_006710397.2:c.1966A>T	XP_006710460.1:p.Lys656Ter
XR_947619.1:n.1347-1233T>A
XR_947620.1:n.1125-1233T>A
XR_947621.1:n.1347-1233T>A
XM_006710397.3:c.1966A>T	XP_006710460.1:p.Lys656Ter
XM_017000507.1:c.1855A>T	XP_016855996.1:p.Lys619Ter
XM_017000508.2:c.1471A>T	XP_016855997.1:p.Lys491Ter
XM_017000509.2:c.1471A>T	XP_016855998.1:p.Lys491Ter
XM_017000510.1:c.1471A>T	XP_016855999.1:p.Lys491Ter
XR_001737686.2:n.692-1233T>A
XR_001737687.1:n.692-1233T>A
XR_001737688.2:n.692-1233T>A
NM_000110.4:c.1966A>T MANE Select	NP_000101.2:p.Lys656Ter