Canonical Allele Identifier: CA1004794325

Gene: DPYD

Linked Data

• dbSNP Id: rs1660994016
• gnomAD v3: 1-97691236-G-A
• gnomAD v4: 1-97691236-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691236G>A , CM000663.2:g.97691236G>A	GRCh38
NC_000001.10:g.98156792G>A , CM000663.1:g.98156792G>A	GRCh37
NC_000001.9:g.97929380G>A	NCBI36
NG_008807.2:g.234824C>T , LRG_722:g.234824C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.762+481C>T MANE Select	ENSP00000359211.3:n.762+481C>T
ENST00000370192.7:c.762+481C>T	ENSP00000359211.3:n.762+481C>T
ENST00000474241.1:n.1007C>T
NM_000110.3:c.762+481C>T , LRG_722t1:c.762+481C>T	NP_000101.2:n.762+481C>T
XM_005270562.3:c.762+481C>T	XP_005270619.2:n.762+481C>T
XM_006710397.2:c.762+481C>T	XP_006710460.1:n.762+481C>T
XM_006710397.3:c.762+481C>T	XP_006710460.1:n.762+481C>T
XM_017000507.1:c.651+481C>T	XP_016855996.1:n.651+481C>T
XM_017000508.2:c.267+481C>T	XP_016855997.1:n.267+481C>T
XM_017000509.2:c.267+481C>T	XP_016855998.1:n.267+481C>T
XM_017000510.1:c.267+481C>T	XP_016855999.1:n.267+481C>T
NM_000110.4:c.762+481C>T MANE Select	NP_000101.2:n.762+481C>T