Canonical Allele Identifier: CA339113760

Gene: SELENON

Linked Data

• COSMIC: COSM343564
• MyVariant Identifiers: chr1:g.26135572G>T (hg19) ; chr1:g.25809081G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25809081G>T , CM000663.2:g.25809081G>T	GRCh38
NC_000001.10:g.26135572G>T , CM000663.1:g.26135572G>T	GRCh37
NC_000001.9:g.26008159G>T	NCBI36
NG_009930.1:g.13906G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.646-14G>T	ENSP00000346109.5:n.646-14G>T
ENST00000494537.2:c.701G>T	ENSP00000508308.1:p.Arg234Leu
ENST00000361547.7:c.803G>T MANE Select	ENSP00000355141.2:p.Arg268Leu
ENST00000354177.8:c.701G>T	ENSP00000346109.4:p.Arg234Leu
ENST00000361547.6:c.803G>T	ENSP00000355141.2:p.Arg268Leu
ENST00000374315.1:c.701G>T	ENSP00000363434.1:p.Arg234Leu
NM_020451.2:c.803G>T	NP_065184.2:p.Arg268Leu
NM_206926.1:c.701G>T	NP_996809.1:p.Arg234Leu
NM_020451.3:c.803G>T MANE Select	NP_065184.2:p.Arg268Leu
NM_206926.2:c.701G>T	NP_996809.1:p.Arg234Leu