Canonical Allele Identifier: CA339117844

Gene: SELENON

Linked Data

• gnomAD v4: 1-25812774-G-C
• MyVariant Identifiers: chr1:g.26139265G>C (hg19) ; chr1:g.25812774G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812774G>C , CM000663.2:g.25812774G>C	GRCh38
NC_000001.10:g.26139265G>C , CM000663.1:g.26139265G>C	GRCh37
NC_000001.9:g.26011852G>C	NCBI36
NG_009930.1:g.17599G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1198G>C	ENSP00000346109.5:p.Asp400His
ENST00000494537.2:c.1267G>C	ENSP00000508308.1:p.Asp423His
ENST00000361547.7:c.1369G>C MANE Select	ENSP00000355141.2:p.Asp457His
ENST00000354177.8:c.1267G>C	ENSP00000346109.4:p.Asp423His
ENST00000361547.6:c.1369G>C	ENSP00000355141.2:p.Asp457His
ENST00000374315.1:c.1267G>C	ENSP00000363434.1:p.Asp423His
ENST00000494537.1:n.47G>C
ENST00000559265.1:n.255+895G>C
ENST00000630065.2:c.-204G>C	ENSP00000487549.1:n.-204G>C
NM_020451.2:c.1369G>C	NP_065184.2:p.Asp457His
NM_206926.1:c.1267G>C	NP_996809.1:p.Asp423His
NM_020451.3:c.1369G>C MANE Select	NP_065184.2:p.Asp457His
NM_206926.2:c.1267G>C	NP_996809.1:p.Asp423His