Canonical Allele Identifier: CA696628

Gene: SELENON

Linked Data

• dbSNP Id: rs761569784
• ExAC: 1:26135498 T / C
• gnomAD v2: 1-26135498-T-C
• gnomAD v4: 1-25809007-T-C
• MyVariant Identifiers: chr1:g.26135498T>C (hg19) ; chr1:g.25809007T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809007T>C , CM000663.2:g.25809007T>C	GRCh38
NC_000001.10:g.26135498T>C , CM000663.1:g.26135498T>C	GRCh37
NC_000001.9:g.26008085T>C	NCBI36
NG_009930.1:g.13832T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.646-88T>C	ENSP00000346109.5:n.646-88T>C
ENST00000494537.2:c.646-19T>C	ENSP00000508308.1:n.646-19T>C
ENST00000361547.7:c.748-19T>C MANE Select	ENSP00000355141.2:n.748-19T>C
ENST00000354177.8:c.646-19T>C	ENSP00000346109.4:n.646-19T>C
ENST00000361547.6:c.748-19T>C	ENSP00000355141.2:n.748-19T>C
ENST00000374315.1:c.646-19T>C	ENSP00000363434.1:n.646-19T>C
NM_020451.2:c.748-19T>C	NP_065184.2:n.748-19T>C
NM_206926.1:c.646-19T>C	NP_996809.1:n.646-19T>C
NM_020451.3:c.748-19T>C MANE Select	NP_065184.2:n.748-19T>C
NM_206926.2:c.646-19T>C	NP_996809.1:n.646-19T>C