Canonical Allele Identifier: CA27624432

Gene: DPYD

Linked Data

• dbSNP Id: rs888150402
• MyVariant Identifiers: chr1:g.98157109A>C (hg19) ; chr1:g.97691553A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691553A>C , CM000663.2:g.97691553A>C	GRCh38
NC_000001.10:g.98157109A>C , CM000663.1:g.98157109A>C	GRCh37
NC_000001.9:g.97929697A>C	NCBI36
NG_008807.2:g.234507T>G , LRG_722:g.234507T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+164T>G MANE Select	ENSP00000359211.3:n.762+164T>G
ENST00000370192.7:c.762+164T>G	ENSP00000359211.3:n.762+164T>G
ENST00000474241.1:n.690T>G
NM_000110.3:c.762+164T>G , LRG_722t1:c.762+164T>G	NP_000101.2:n.762+164T>G
XM_005270562.3:c.762+164T>G	XP_005270619.2:n.762+164T>G
XM_006710397.2:c.762+164T>G	XP_006710460.1:n.762+164T>G
XM_006710397.3:c.762+164T>G	XP_006710460.1:n.762+164T>G
XM_017000507.1:c.651+164T>G	XP_016855996.1:n.651+164T>G
XM_017000508.2:c.267+164T>G	XP_016855997.1:n.267+164T>G
XM_017000509.2:c.267+164T>G	XP_016855998.1:n.267+164T>G
XM_017000510.1:c.267+164T>G	XP_016855999.1:n.267+164T>G
NM_000110.4:c.762+164T>G MANE Select	NP_000101.2:n.762+164T>G