Canonical Allele Identifier: CA341380148

Gene: DPYD

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97883328C>G , CM000663.2:g.97883328C>G	GRCh38
NC_000001.10:g.98348884C>G , CM000663.1:g.98348884C>G	GRCh37
NC_000001.9:g.98121472C>G	NCBI36
NG_008807.2:g.42732G>C , LRG_722:g.42732G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.86G>C MANE Select	ENSP00000359211.3:p.Cys29Ser
ENST00000646851.1:n.735G>C
ENST00000306031.5:c.86G>C	ENSP00000307107.5:p.Cys29Ser
ENST00000370192.7:c.86G>C	ENSP00000359211.3:p.Cys29Ser
ENST00000460019.1:n.161G>C
NM_000110.3:c.86G>C , LRG_722t1:c.86G>C	NP_000101.2:p.Cys29Ser
NM_001160301.1:c.86G>C , LRG_722t2:c.86G>C	NP_001153773.1:p.Cys29Ser
XM_005270562.3:c.86G>C	XP_005270619.2:p.Cys29Ser
XM_006710397.2:c.86G>C	XP_006710460.1:p.Cys29Ser
XM_006710397.3:c.86G>C	XP_006710460.1:p.Cys29Ser
XM_017000507.1:c.39+37556G>C	XP_016855996.1:n.39+37556G>C
XM_017000508.2:c.-625G>C	XP_016855997.1:n.-625G>C
XM_017000509.2:c.-523G>C	XP_016855998.1:n.-523G>C
XM_017000510.1:c.-459+37556G>C	XP_016855999.1:n.-459+37556G>C
XR_001737014.1:n.223G>C
NM_000110.4:c.86G>C MANE Select	NP_000101.2:p.Cys29Ser