Canonical Allele Identifier: CA341375846

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97848000A>C (hg19) ; chr1:g.97382444A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382444A>C , CM000663.2:g.97382444A>C	GRCh38
NC_000001.10:g.97848000A>C , CM000663.1:g.97848000A>C	GRCh37
NC_000001.9:g.97620588A>C	NCBI36
NG_008807.2:g.543616T>G , LRG_722:g.543616T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1923T>G MANE Select	ENSP00000359211.3:p.Ile641Met
ENST00000370192.7:c.1923T>G	ENSP00000359211.3:p.Ile641Met
NM_000110.3:c.1923T>G , LRG_722t1:c.1923T>G	NP_000101.2:p.Ile641Met
XM_005270562.3:c.1707T>G	XP_005270619.2:p.Ile569Met
XM_006710397.2:c.1923T>G	XP_006710460.1:p.Ile641Met
XR_947619.1:n.1347-1190A>C
XR_947620.1:n.1125-1190A>C
XR_947621.1:n.1347-1190A>C
XM_006710397.3:c.1923T>G	XP_006710460.1:p.Ile641Met
XM_017000507.1:c.1812T>G	XP_016855996.1:p.Ile604Met
XM_017000508.2:c.1428T>G	XP_016855997.1:p.Ile476Met
XM_017000509.2:c.1428T>G	XP_016855998.1:p.Ile476Met
XM_017000510.1:c.1428T>G	XP_016855999.1:p.Ile476Met
XR_001737686.2:n.692-1190A>C
XR_001737687.1:n.692-1190A>C
XR_001737688.2:n.692-1190A>C
NM_000110.4:c.1923T>G MANE Select	NP_000101.2:p.Ile641Met