Canonical Allele Identifier: CA2741458717
Gene: SELENOS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.101273755del , CM000677.2:g.101273755del GRCh38
NC_000015.9:g.101813960del , CM000677.1:g.101813960del GRCh37
NC_000015.8:g.99631483del NCBI36
NG_013322.1:g.8743del

Transcript Alleles

HGVS Amino-acid change
ENST00000526049.6:c.484+667del MANE Select ENSP00000433541.1:n.484+667del
ENST00000398226.7:c.484+667del ENSP00000381282.3:n.484+667del
ENST00000526043.1:n.1777+667del
ENST00000526049.5:c.484+667del ENSP00000433541.1:n.484+667del
ENST00000528346.1:c.604+667del ENSP00000434842.1:n.604+667del
ENST00000531964.5:c.415+667del ENSP00000433803.1:n.415+667del
NM_018445.5:c.484+667del NP_060915.2:n.484+667del
NM_203472.2:c.484+667del NP_982298.2:n.484+667del
NM_018445.6:c.484+667del MANE Select NP_060915.2:n.484+667del
NM_203472.3:c.484+667del NP_982298.2:n.484+667del