Canonical Allele Identifier: CA2573132210
Gene: SELENON HGNC NCBI

Linked Data

ClinVar Variation Id: 1528944
ClinVar RCV Id: RCV002086902
dbSNP Id: rs2124447905
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809014del , CM000663.2:g.25809014del GRCh38
NC_000001.10:g.26135505del , CM000663.1:g.26135505del GRCh37
NC_000001.9:g.26008092del NCBI36
NG_009930.1:g.13839del

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.646-81del ENSP00000346109.5:n.646-81del
ENST00000494537.2:c.646-12del ENSP00000508308.1:n.646-12del
ENST00000361547.7:c.748-12del MANE Select ENSP00000355141.2:n.748-12del
ENST00000354177.8:c.646-12del ENSP00000346109.4:n.646-12del
ENST00000361547.6:c.748-12del ENSP00000355141.2:n.748-12del
ENST00000374315.1:c.646-12del ENSP00000363434.1:n.646-12del
NM_020451.2:c.748-12del NP_065184.2:n.748-12del
NM_206926.1:c.646-12del NP_996809.1:n.646-12del
NM_020451.3:c.748-12del MANE Select NP_065184.2:n.748-12del
NM_206926.2:c.646-12del NP_996809.1:n.646-12del
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