Canonical Allele Identifier: CA15071019
Gene: DPYD HGNC NCBI

Linked Data

dbSNP Id: rs6685859
gnomAD v2: 1-97822769-G-C
gnomAD v3: 1-97357213-G-C
gnomAD v4: 1-97357213-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97357213G>C , CM000663.2:g.97357213G>C GRCh38
NC_000001.10:g.97822769G>C , CM000663.1:g.97822769G>C GRCh37
NC_000001.9:g.97595357G>C NCBI36
NG_008807.2:g.568847C>G , LRG_722:g.568847C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370192.8:c.2058+16348C>G MANE Select ENSP00000359211.3:n.2058+16348C>G
ENST00000370192.7:c.2058+16348C>G ENSP00000359211.3:n.2058+16348C>G
NM_000110.3:c.2058+16348C>G , LRG_722t1:c.2058+16348C>G NP_000101.2:n.2058+16348C>G
XM_005270562.3:c.1842+16348C>G XP_005270619.2:n.1842+16348C>G
XM_006710397.2:c.2058+16348C>G XP_006710460.1:n.2058+16348C>G
XR_947619.1:n.921-9785G>C
XR_947620.1:n.921-9785G>C
XR_947621.1:n.921-9785G>C
XM_006710397.3:c.2058+16348C>G XP_006710460.1:n.2058+16348C>G
XM_017000507.1:c.1947+16348C>G XP_016855996.1:n.1947+16348C>G
XM_017000508.2:c.1563+16348C>G XP_016855997.1:n.1563+16348C>G
XM_017000509.2:c.1563+16348C>G XP_016855998.1:n.1563+16348C>G
XM_017000510.1:c.1563+16348C>G XP_016855999.1:n.1563+16348C>G
NM_000110.4:c.2058+16348C>G MANE Select NP_000101.2:n.2058+16348C>G