Canonical Allele Identifier: CA15089324

Gene: SELENON

Linked Data

• ClinVar Variation Id: 1264793
• ClinVar RCV Id: RCV001677038
• dbSNP Id: rs72877458
• gnomAD v2: 1-26135856-T-C
• gnomAD v3: 1-25809365-T-C
• gnomAD v4: 1-25809365-T-C
• MyVariant Identifiers: chr1:g.26135856T>C (hg19) ; chr1:g.25809365T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809365T>C , CM000663.2:g.25809365T>C	GRCh38
NC_000001.10:g.26135856T>C , CM000663.1:g.26135856T>C	GRCh37
NC_000001.9:g.26008443T>C	NCBI36
NG_009930.1:g.14190T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.701+215T>C	ENSP00000346109.5:n.701+215T>C
ENST00000494537.2:c.770+215T>C	ENSP00000508308.1:n.770+215T>C
ENST00000361547.7:c.872+215T>C MANE Select	ENSP00000355141.2:n.872+215T>C
ENST00000354177.8:c.770+215T>C	ENSP00000346109.4:n.770+215T>C
ENST00000361547.6:c.872+215T>C	ENSP00000355141.2:n.872+215T>C
ENST00000374315.1:c.770+215T>C	ENSP00000363434.1:n.770+215T>C
NM_020451.2:c.872+215T>C	NP_065184.2:n.872+215T>C
NM_206926.1:c.770+215T>C	NP_996809.1:n.770+215T>C
NM_020451.3:c.872+215T>C MANE Select	NP_065184.2:n.872+215T>C
NM_206926.2:c.770+215T>C	NP_996809.1:n.770+215T>C