Canonical Allele Identifier: CA339118950

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26140381G>C (hg19) ; chr1:g.25813890G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25813890G>C , CM000663.2:g.25813890G>C	GRCh38
NC_000001.10:g.26140381G>C , CM000663.1:g.26140381G>C	GRCh37
NC_000001.9:g.26012968G>C	NCBI36
NG_009930.1:g.18715G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1226G>C	ENSP00000346109.5:p.Arg409Pro
ENST00000494537.2:c.1384G>C	ENSP00000508308.1:p.Gly462Arg
ENST00000361547.7:c.1397G>C MANE Select	ENSP00000355141.2:p.Arg466Pro
ENST00000354177.8:c.1295G>C	ENSP00000346109.4:p.Arg432Pro
ENST00000361547.6:c.1397G>C	ENSP00000355141.2:p.Arg466Pro
ENST00000374315.1:c.1295G>C	ENSP00000363434.1:p.Arg432Pro
ENST00000494537.1:n.164G>C
ENST00000559265.1:n.255+2011G>C
ENST00000630065.2:c.-176G>C	ENSP00000487549.1:n.-176G>C
NM_020451.2:c.1397G>C	NP_065184.2:p.Arg466Pro
NM_206926.1:c.1295G>C	NP_996809.1:p.Arg432Pro
NM_020451.3:c.1397G>C MANE Select	NP_065184.2:p.Arg466Pro
NM_206926.2:c.1295G>C	NP_996809.1:p.Arg432Pro