Canonical Allele Identifier: CA10802534

Gene: SELENON

Linked Data

• ClinVar Variation Id: 680776
• ClinVar RCV Id: RCV000840578
• dbSNP Id: rs7542128
• gnomAD v2: 1-26135913-T-C
• gnomAD v3: 1-25809422-T-C
• gnomAD v4: 1-25809422-T-C
• MyVariant Identifiers: chr1:g.26135913T>C (hg19) ; chr1:g.25809422T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809422T>C , CM000663.2:g.25809422T>C	GRCh38
NC_000001.10:g.26135913T>C , CM000663.1:g.26135913T>C	GRCh37
NC_000001.9:g.26008500T>C	NCBI36
NG_009930.1:g.14247T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.702-261T>C	ENSP00000346109.5:n.702-261T>C
ENST00000494537.2:c.771-261T>C	ENSP00000508308.1:n.771-261T>C
ENST00000361547.7:c.873-261T>C MANE Select	ENSP00000355141.2:n.873-261T>C
ENST00000354177.8:c.771-261T>C	ENSP00000346109.4:n.771-261T>C
ENST00000361547.6:c.873-261T>C	ENSP00000355141.2:n.873-261T>C
ENST00000374315.1:c.771-261T>C	ENSP00000363434.1:n.771-261T>C
NM_020451.2:c.873-261T>C	NP_065184.2:n.873-261T>C
NM_206926.1:c.771-261T>C	NP_996809.1:n.771-261T>C
NM_020451.3:c.873-261T>C MANE Select	NP_065184.2:n.873-261T>C
NM_206926.2:c.771-261T>C	NP_996809.1:n.771-261T>C