Canonical Allele Identifier: CA2646707039

Gene: DPYD

Linked Data

• gnomAD v4: 1-97691637-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691637G>T , CM000663.2:g.97691637G>T	GRCh38
NC_000001.10:g.98157193G>T , CM000663.1:g.98157193G>T	GRCh37
NC_000001.9:g.97929781G>T	NCBI36
NG_008807.2:g.234423C>A , LRG_722:g.234423C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+80C>A MANE Select	ENSP00000359211.3:n.762+80C>A
ENST00000370192.7:c.762+80C>A	ENSP00000359211.3:n.762+80C>A
ENST00000474241.1:n.606C>A
NM_000110.3:c.762+80C>A , LRG_722t1:c.762+80C>A	NP_000101.2:n.762+80C>A
XM_005270562.3:c.762+80C>A	XP_005270619.2:n.762+80C>A
XM_006710397.2:c.762+80C>A	XP_006710460.1:n.762+80C>A
XM_006710397.3:c.762+80C>A	XP_006710460.1:n.762+80C>A
XM_017000507.1:c.651+80C>A	XP_016855996.1:n.651+80C>A
XM_017000508.2:c.267+80C>A	XP_016855997.1:n.267+80C>A
XM_017000509.2:c.267+80C>A	XP_016855998.1:n.267+80C>A
XM_017000510.1:c.267+80C>A	XP_016855999.1:n.267+80C>A
NM_000110.4:c.762+80C>A MANE Select	NP_000101.2:n.762+80C>A