Canonical Allele Identifier: CA339117671

Gene: SELENON

Linked Data

• MyVariant Identifiers: chr1:g.26139181T>G (hg19) ; chr1:g.25812690T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812690T>G , CM000663.2:g.25812690T>G	GRCh38
NC_000001.10:g.26139181T>G , CM000663.1:g.26139181T>G	GRCh37
NC_000001.9:g.26011768T>G	NCBI36
NG_009930.1:g.17515T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1114T>G	ENSP00000346109.5:p.Ser372Ala
ENST00000494537.2:c.1183T>G	ENSP00000508308.1:p.Ser395Ala
ENST00000361547.7:c.1285T>G MANE Select	ENSP00000355141.2:p.Ser429Ala
ENST00000354177.8:c.1183T>G	ENSP00000346109.4:p.Ser395Ala
ENST00000361547.6:c.1285T>G	ENSP00000355141.2:p.Ser429Ala
ENST00000374315.1:c.1183T>G	ENSP00000363434.1:p.Ser395Ala
ENST00000559265.1:n.255+811T>G
ENST00000630065.2:c.-288T>G	ENSP00000487549.1:n.-288T>G
NM_020451.2:c.1285T>G	NP_065184.2:p.Ser429Ala
NM_206926.1:c.1183T>G	NP_996809.1:p.Ser395Ala
NM_020451.3:c.1285T>G MANE Select	NP_065184.2:p.Ser429Ala
NM_206926.2:c.1183T>G	NP_996809.1:p.Ser395Ala