Canonical Allele Identifier: CA1004794514

Gene: DPYD

Linked Data

• dbSNP Id: rs1292453820
• gnomAD v3: 1-97691711-A-C
• gnomAD v4: 1-97691711-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691711A>C , CM000663.2:g.97691711A>C	GRCh38
NC_000001.10:g.98157267A>C , CM000663.1:g.98157267A>C	GRCh37
NC_000001.9:g.97929855A>C	NCBI36
NG_008807.2:g.234349T>G , LRG_722:g.234349T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.762+6T>G MANE Select	ENSP00000359211.3:n.762+6T>G
ENST00000370192.7:c.762+6T>G	ENSP00000359211.3:n.762+6T>G
ENST00000474241.1:n.532T>G
NM_000110.3:c.762+6T>G , LRG_722t1:c.762+6T>G	NP_000101.2:n.762+6T>G
XM_005270562.3:c.762+6T>G	XP_005270619.2:n.762+6T>G
XM_006710397.2:c.762+6T>G	XP_006710460.1:n.762+6T>G
XM_006710397.3:c.762+6T>G	XP_006710460.1:n.762+6T>G
XM_017000507.1:c.651+6T>G	XP_016855996.1:n.651+6T>G
XM_017000508.2:c.267+6T>G	XP_016855997.1:n.267+6T>G
XM_017000509.2:c.267+6T>G	XP_016855998.1:n.267+6T>G
XM_017000510.1:c.267+6T>G	XP_016855999.1:n.267+6T>G
NM_000110.4:c.762+6T>G MANE Select	NP_000101.2:n.762+6T>G