Canonical Allele Identifier: CA27624480

Gene: DPYD

Linked Data

• dbSNP Id: rs34213322
• MyVariant Identifiers: chr1:g.98157141_98157142insA (hg19) ; chr1:g.97691585_97691586insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97691585_97691586insA , CM000663.2:g.97691585_97691586insA	GRCh38
NC_000001.10:g.98157141_98157142insA , CM000663.1:g.98157141_98157142insA	GRCh37
NC_000001.9:g.97929729_97929730insA	NCBI36
NG_008807.2:g.234474_234475insT , LRG_722:g.234474_234475insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000370192.8:c.762+131_762+132insT MANE Select	ENSP00000359211.3:n.762+131_762+132insT
ENST00000370192.7:c.762+131_762+132insT	ENSP00000359211.3:n.762+131_762+132insT
ENST00000474241.1:n.657_658insT
NM_000110.3:c.762+131_762+132insT , LRG_722t1:c.762+131_762+132insT	NP_000101.2:n.762+131_762+132insT
XM_005270562.3:c.762+131_762+132insT	XP_005270619.2:n.762+131_762+132insT
XM_006710397.2:c.762+131_762+132insT	XP_006710460.1:n.762+131_762+132insT
XM_006710397.3:c.762+131_762+132insT	XP_006710460.1:n.762+131_762+132insT
XM_017000507.1:c.651+131_651+132insT	XP_016855996.1:n.651+131_651+132insT
XM_017000508.2:c.267+131_267+132insT	XP_016855997.1:n.267+131_267+132insT
XM_017000509.2:c.267+131_267+132insT	XP_016855998.1:n.267+131_267+132insT
XM_017000510.1:c.267+131_267+132insT	XP_016855999.1:n.267+131_267+132insT
NM_000110.4:c.762+131_762+132insT MANE Select	NP_000101.2:n.762+131_762+132insT