Canonical Allele Identifier: CA963212

Gene: DPYD

Linked Data

• dbSNP Id: rs762420899
• ExAC: 1:97915612 T / A
• gnomAD v2: 1-97915612-T-A
• gnomAD v4: 1-97450056-T-A
• MyVariant Identifiers: chr1:g.97915612T>A (hg19) ; chr1:g.97450056T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450056T>A , CM000663.2:g.97450056T>A	GRCh38
NC_000001.10:g.97915612T>A , CM000663.1:g.97915612T>A	GRCh37
NC_000001.9:g.97688200T>A	NCBI36
NG_008807.2:g.476004A>T , LRG_722:g.476004A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1905+3A>T MANE Select	ENSP00000359211.3:n.1905+3A>T
ENST00000370192.7:c.1905+3A>T	ENSP00000359211.3:n.1905+3A>T
NM_000110.3:c.1905+3A>T , LRG_722t1:c.1905+3A>T	NP_000101.2:n.1905+3A>T
XM_005270562.3:c.1689+3A>T	XP_005270619.2:n.1689+3A>T
XM_006710397.2:c.1905+3A>T	XP_006710460.1:n.1905+3A>T
XM_006710397.3:c.1905+3A>T	XP_006710460.1:n.1905+3A>T
XM_017000507.1:c.1794+3A>T	XP_016855996.1:n.1794+3A>T
XM_017000508.2:c.1410+3A>T	XP_016855997.1:n.1410+3A>T
XM_017000509.2:c.1410+3A>T	XP_016855998.1:n.1410+3A>T
XM_017000510.1:c.1410+3A>T	XP_016855999.1:n.1410+3A>T
NM_000110.4:c.1905+3A>T MANE Select	NP_000101.2:n.1905+3A>T