Canonical Allele Identifier: CA1873789208
Gene: ORM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114325805A= , CM000671.2:g.114325805A= GRCh38
NC_000009.11:g.117088085A= , CM000671.1:g.117088085A= GRCh37
NC_000009.10:g.116127906A= NCBI36
NG_012108.1:g.7783A=

Transcript Alleles

HGVS Amino-acid change
ENST00000259396.9:c.541-487A= MANE Select ENSP00000259396.8:n.541-487A=
ENST00000259396.8:c.541-487A= ENSP00000259396.8:n.541-487A=
NM_000607.2:c.541-487A= NP_000598.2:n.541-487A=
NM_000607.3:c.541-487A= NP_000598.2:n.541-487A=
NM_000607.4:c.541-487A= MANE Select NP_000598.2:n.541-487A=