Canonical Allele Identifier: CA341375947

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97915635T>G (hg19) ; chr1:g.97450079T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450079T>G , CM000663.2:g.97450079T>G	GRCh38
NC_000001.10:g.97915635T>G , CM000663.1:g.97915635T>G	GRCh37
NC_000001.9:g.97688223T>G	NCBI36
NG_008807.2:g.475981A>C , LRG_722:g.475981A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1885A>C MANE Select	ENSP00000359211.3:p.Lys629Gln
ENST00000370192.7:c.1885A>C	ENSP00000359211.3:p.Lys629Gln
NM_000110.3:c.1885A>C , LRG_722t1:c.1885A>C	NP_000101.2:p.Lys629Gln
XM_005270562.3:c.1669A>C	XP_005270619.2:p.Lys557Gln
XM_006710397.2:c.1885A>C	XP_006710460.1:p.Lys629Gln
XM_006710397.3:c.1885A>C	XP_006710460.1:p.Lys629Gln
XM_017000507.1:c.1774A>C	XP_016855996.1:p.Lys592Gln
XM_017000508.2:c.1390A>C	XP_016855997.1:p.Lys464Gln
XM_017000509.2:c.1390A>C	XP_016855998.1:p.Lys464Gln
XM_017000510.1:c.1390A>C	XP_016855999.1:p.Lys464Gln
NM_000110.4:c.1885A>C MANE Select	NP_000101.2:p.Lys629Gln