Canonical Allele Identifier: CA1182927954

Gene: DPYD

Linked Data

• dbSNP Id: rs981735823
• gnomAD v4: 1-97573700-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97573700C>G , CM000663.2:g.97573700C>G	GRCh38
NC_000001.10:g.98039256C>G , CM000663.1:g.98039256C>G	GRCh37
NC_000001.9:g.97811844C>G	NCBI36
NG_008807.2:g.352360G>C , LRG_722:g.352360G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.1339+60G>C MANE Select	ENSP00000359211.3:n.1339+60G>C
ENST00000370192.7:c.1339+60G>C	ENSP00000359211.3:n.1339+60G>C
NM_000110.3:c.1339+60G>C , LRG_722t1:c.1339+60G>C	NP_000101.2:n.1339+60G>C
XM_005270562.3:c.1339+60G>C	XP_005270619.2:n.1339+60G>C
XM_006710397.2:c.1339+60G>C	XP_006710460.1:n.1339+60G>C
XM_006710397.3:c.1339+60G>C	XP_006710460.1:n.1339+60G>C
XM_017000507.1:c.1228+60G>C	XP_016855996.1:n.1228+60G>C
XM_017000508.2:c.844+60G>C	XP_016855997.1:n.844+60G>C
XM_017000509.2:c.844+60G>C	XP_016855998.1:n.844+60G>C
XM_017000510.1:c.844+60G>C	XP_016855999.1:n.844+60G>C
NM_000110.4:c.1339+60G>C MANE Select	NP_000101.2:n.1339+60G>C