Canonical Allele Identifier: CA2696663526

Gene: DPYD

Linked Data

• dbSNP Id: rs2101565737

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97382616A>G , CM000663.2:g.97382616A>G	GRCh38
NC_000001.10:g.97848172A>G , CM000663.1:g.97848172A>G	GRCh37
NC_000001.9:g.97620760A>G	NCBI36
NG_008807.2:g.543444T>C , LRG_722:g.543444T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1906-155T>C MANE Select	ENSP00000359211.3:n.1906-155T>C
ENST00000370192.7:c.1906-155T>C	ENSP00000359211.3:n.1906-155T>C
NM_000110.3:c.1906-155T>C , LRG_722t1:c.1906-155T>C	NP_000101.2:n.1906-155T>C
XM_005270562.3:c.1690-155T>C	XP_005270619.2:n.1690-155T>C
XM_006710397.2:c.1906-155T>C	XP_006710460.1:n.1906-155T>C
XR_947619.1:n.1347-1018A>G
XR_947620.1:n.1125-1018A>G
XR_947621.1:n.1347-1018A>G
XM_006710397.3:c.1906-155T>C	XP_006710460.1:n.1906-155T>C
XM_017000507.1:c.1795-155T>C	XP_016855996.1:n.1795-155T>C
XM_017000508.2:c.1411-155T>C	XP_016855997.1:n.1411-155T>C
XM_017000509.2:c.1411-155T>C	XP_016855998.1:n.1411-155T>C
XM_017000510.1:c.1411-155T>C	XP_016855999.1:n.1411-155T>C
XR_001737686.2:n.692-1018A>G
XR_001737687.1:n.692-1018A>G
XR_001737688.2:n.692-1018A>G
NM_000110.4:c.1906-155T>C MANE Select	NP_000101.2:n.1906-155T>C