Canonical Allele Identifier: CA339117688

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139188T>C (hg19) ; chr1:g.25812697T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812697T>C , CM000663.2:g.25812697T>C	GRCh38
NC_000001.10:g.26139188T>C , CM000663.1:g.26139188T>C	GRCh37
NC_000001.9:g.26011775T>C	NCBI36
NG_009930.1:g.17522T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1121T>C	ENSP00000346109.5:p.Leu374Ser
ENST00000494537.2:c.1190T>C	ENSP00000508308.1:p.Leu397Ser
ENST00000361547.7:c.1292T>C MANE Select	ENSP00000355141.2:p.Leu431Ser
ENST00000354177.8:c.1190T>C	ENSP00000346109.4:p.Leu397Ser
ENST00000361547.6:c.1292T>C	ENSP00000355141.2:p.Leu431Ser
ENST00000374315.1:c.1190T>C	ENSP00000363434.1:p.Leu397Ser
ENST00000559265.1:n.255+818T>C
ENST00000630065.2:c.-281T>C	ENSP00000487549.1:n.-281T>C
NM_020451.2:c.1292T>C	NP_065184.2:p.Leu431Ser
NM_206926.1:c.1190T>C	NP_996809.1:p.Leu397Ser
NM_020451.3:c.1292T>C MANE Select	NP_065184.2:p.Leu431Ser
NM_206926.2:c.1190T>C	NP_996809.1:p.Leu397Ser