Canonical Allele Identifier: CA1873789201
Gene: ORM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325791T= , CM000671.2:g.114325791T= GRCh38
NC_000009.11:g.117088071T= , CM000671.1:g.117088071T= GRCh37
NC_000009.10:g.116127892T= NCBI36
NG_012108.1:g.7769T=

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-501T= MANE Select ENSP00000259396.8:n.541-501T=
ENST00000259396.8:c.541-501T= ENSP00000259396.8:n.541-501T=
NM_000607.2:c.541-501T= NP_000598.2:n.541-501T=
NM_000607.3:c.541-501T= NP_000598.2:n.541-501T=
NM_000607.4:c.541-501T= MANE Select NP_000598.2:n.541-501T=