Canonical Allele Identifier: CA1807671384
Gene: DPYS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.104379424T= , CM000670.2:g.104379424T= GRCh38
NC_000008.10:g.105391652T= , CM000670.1:g.105391652T= GRCh37
NC_000008.9:g.105460828T= NCBI36
NG_008840.1:g.92626A=
NG_008840.2:g.92626A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351513.6:c.*434A= ENSP00000276651.2:n.*434A=
ENST00000521601.1:n.328+1760A=
NM_001385.2:c.*434A= NP_001376.1:n.*434A=