Canonical Allele Identifier: CA2646706220

Gene: DPYD

Linked Data

• gnomAD v4: 1-97549523-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97549523G>C , CM000663.2:g.97549523G>C	GRCh38
NC_000001.10:g.98015079G>C , CM000663.1:g.98015079G>C	GRCh37
NC_000001.9:g.97787667G>C	NCBI36
NG_008807.2:g.376537C>G , LRG_722:g.376537C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1524+37C>G MANE Select	ENSP00000359211.3:n.1524+37C>G
ENST00000370192.7:c.1524+37C>G	ENSP00000359211.3:n.1524+37C>G
NM_000110.3:c.1524+37C>G , LRG_722t1:c.1524+37C>G	NP_000101.2:n.1524+37C>G
XM_005270562.3:c.1524+37C>G	XP_005270619.2:n.1524+37C>G
XM_006710397.2:c.1524+37C>G	XP_006710460.1:n.1524+37C>G
XM_006710397.3:c.1524+37C>G	XP_006710460.1:n.1524+37C>G
XM_017000507.1:c.1413+37C>G	XP_016855996.1:n.1413+37C>G
XM_017000508.2:c.1029+37C>G	XP_016855997.1:n.1029+37C>G
XM_017000509.2:c.1029+37C>G	XP_016855998.1:n.1029+37C>G
XM_017000510.1:c.1029+37C>G	XP_016855999.1:n.1029+37C>G
NM_000110.4:c.1524+37C>G MANE Select	NP_000101.2:n.1524+37C>G