Canonical Allele Identifier: CA419140939

Gene: DPYD

Linked Data

• MyVariant Identifiers: chr1:g.97847964A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382408A>C , CM000663.2:g.97382408A>C	GRCh38
NC_000001.10:g.97847964A>C , CM000663.1:g.97847964A>C	GRCh37
NC_000001.9:g.97620552A>C	NCBI36
NG_008807.2:g.543652T>G , LRG_722:g.543652T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1959T>G MANE Select	ENSP00000359211.3:p.Leu653=
ENST00000370192.7:c.1959T>G	ENSP00000359211.3:p.Leu653=
NM_000110.3:c.1959T>G , LRG_722t1:c.1959T>G	NP_000101.2:p.Leu653=
XM_005270562.3:c.1743T>G	XP_005270619.2:p.Leu581=
XM_006710397.2:c.1959T>G	XP_006710460.1:p.Leu653=
XR_947619.1:n.1347-1226A>C
XR_947620.1:n.1125-1226A>C
XR_947621.1:n.1347-1226A>C
XM_006710397.3:c.1959T>G	XP_006710460.1:p.Leu653=
XM_017000507.1:c.1848T>G	XP_016855996.1:p.Leu616=
XM_017000508.2:c.1464T>G	XP_016855997.1:p.Leu488=
XM_017000509.2:c.1464T>G	XP_016855998.1:p.Leu488=
XM_017000510.1:c.1464T>G	XP_016855999.1:p.Leu488=
XR_001737686.2:n.692-1226A>C
XR_001737687.1:n.692-1226A>C
XR_001737688.2:n.692-1226A>C
NM_000110.4:c.1959T>G MANE Select	NP_000101.2:p.Leu653=