Canonical Allele Identifier: CA1004806780

Gene: DPYD

Linked Data

• dbSNP Id: rs1672313755
• gnomAD v3: 1-97883193-G-A
• gnomAD v4: 1-97883193-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97883193G>A , CM000663.2:g.97883193G>A	GRCh38
NC_000001.10:g.98348749G>A , CM000663.1:g.98348749G>A	GRCh37
NC_000001.9:g.98121337G>A	NCBI36
NG_008807.2:g.42867C>T , LRG_722:g.42867C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.150+71C>T MANE Select	ENSP00000359211.3:n.150+71C>T
ENST00000306031.5:c.150+71C>T	ENSP00000307107.5:n.150+71C>T
ENST00000370192.7:c.150+71C>T	ENSP00000359211.3:n.150+71C>T
ENST00000460019.1:n.225+71C>T
NM_000110.3:c.150+71C>T , LRG_722t1:c.150+71C>T	NP_000101.2:n.150+71C>T
NM_001160301.1:c.150+71C>T , LRG_722t2:c.150+71C>T	NP_001153773.1:n.150+71C>T
XM_005270562.3:c.150+71C>T	XP_005270619.2:n.150+71C>T
XM_006710397.2:c.150+71C>T	XP_006710460.1:n.150+71C>T
XM_006710397.3:c.150+71C>T	XP_006710460.1:n.150+71C>T
XM_017000507.1:c.39+37691C>T	XP_016855996.1:n.39+37691C>T
XM_017000508.2:c.-561+71C>T	XP_016855997.1:n.-561+71C>T
XM_017000509.2:c.-459+71C>T	XP_016855998.1:n.-459+71C>T
XM_017000510.1:c.-459+37691C>T	XP_016855999.1:n.-459+37691C>T
XR_001737014.1:n.287+71C>T
NM_000110.4:c.150+71C>T MANE Select	NP_000101.2:n.150+71C>T