Canonical Allele Identifier: CA1807671387
Gene: DPYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379427G= , CM000670.2:g.104379427G= GRCh38
NC_000008.10:g.105391655G= , CM000670.1:g.105391655G= GRCh37
NC_000008.9:g.105460831G= NCBI36
NG_008840.1:g.92623C=
NG_008840.2:g.92623C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351513.6:c.*431C= ENSP00000276651.2:n.*431C=
ENST00000521601.1:n.328+1757C=
NM_001385.2:c.*431C= NP_001376.1:n.*431C=