Canonical Allele Identifier: CA963211

Gene: DPYD

Linked Data

• dbSNP Id: rs760156122
• ExAC: 1:97915612 T / TAA
• gnomAD v2: 1-97915612-T-TAA
• gnomAD v4: 1-97450056-T-TAA
• MyVariant Identifiers: chr1:g.97915612_97915613insAA (hg19) ; chr1:g.97450056_97450057insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97450057_97450058insAA , CM000663.2:g.97450057_97450058insAA	GRCh38
NC_000001.10:g.97915613_97915614insAA , CM000663.1:g.97915613_97915614insAA	GRCh37
NC_000001.9:g.97688201_97688202insAA	NCBI36
NG_008807.2:g.476003_476004insTT , LRG_722:g.476003_476004insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.1905+2_1905+3insTT MANE Select	ENSP00000359211.3:n.1905+2_1905+3insTT
ENST00000370192.7:c.1905+2_1905+3insTT	ENSP00000359211.3:n.1905+2_1905+3insTT
NM_000110.3:c.1905+2_1905+3insTT , LRG_722t1:c.1905+2_1905+3insTT	NP_000101.2:n.1905+2_1905+3insTT
XM_005270562.3:c.1689+2_1689+3insTT	XP_005270619.2:n.1689+2_1689+3insTT
XM_006710397.2:c.1905+2_1905+3insTT	XP_006710460.1:n.1905+2_1905+3insTT
XM_006710397.3:c.1905+2_1905+3insTT	XP_006710460.1:n.1905+2_1905+3insTT
XM_017000507.1:c.1794+2_1794+3insTT	XP_016855996.1:n.1794+2_1794+3insTT
XM_017000508.2:c.1410+2_1410+3insTT	XP_016855997.1:n.1410+2_1410+3insTT
XM_017000509.2:c.1410+2_1410+3insTT	XP_016855998.1:n.1410+2_1410+3insTT
XM_017000510.1:c.1410+2_1410+3insTT	XP_016855999.1:n.1410+2_1410+3insTT
NM_000110.4:c.1905+2_1905+3insTT MANE Select	NP_000101.2:n.1905+2_1905+3insTT