Canonical Allele Identifier: CA1399821759
Gene: UROC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.126510622C= , CM000665.2:g.126510622C= GRCh38
NC_000003.11:g.126229465C= , CM000665.1:g.126229465C= GRCh37
NC_000003.10:g.127712155C= NCBI36
NG_016286.1:g.12130G=

Transcript Alleles

HGVS Amino-acid change
ENST00000290868.7:c.257+42G= MANE Select ENSP00000290868.2:n.257+42G=
ENST00000290868.6:c.257+42G= ENSP00000290868.2:n.257+42G=
ENST00000383579.3:c.257+42G= ENSP00000373073.3:n.257+42G=
NM_001165974.1:c.257+42G= NP_001159446.1:n.257+42G=
NM_144639.2:c.257+42G= NP_653240.1:n.257+42G=
NM_144639.3:c.257+42G= MANE Select NP_653240.1:n.257+42G=
NM_001165974.2:c.257+42G= NP_001159446.1:n.257+42G=