Canonical Allele Identifier: CA339105607
Community Standard Title: NM_020451.3(SELENON):c.2T>A (p.Met1Lys)
Gene: SELENON HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25800232T>A , CM000663.2:g.25800232T>A GRCh38
NC_000001.10:g.26126723T>A , CM000663.1:g.26126723T>A GRCh37
NC_000001.9:g.25999310T>A NCBI36
NG_009930.1:g.5057T>A

Transcript Alleles

HGVS Amino-acid Change
NM_020451.3:c.2T>A MANE Select NP_065184.2:p.Met1Lys
ENST00000361547.7:c.2T>A MANE Select ENSP00000355141.2:p.Met1Lys
NM_020451.2:c.2T>A NP_065184.2:p.Met1Lys
NM_206926.1:c.2T>A NP_996809.1:p.Met1Lys
NM_206926.2:c.2T>A NP_996809.1:p.Met1Lys
ENST00000354177.8:c.2T>A ENSP00000346109.4:p.Met1Lys
ENST00000354177.9:c.2T>A ENSP00000346109.5:p.Met1Lys
ENST00000361547.6:c.2T>A ENSP00000355141.2:p.Met1Lys
ENST00000374315.1:c.2T>A ENSP00000363434.1:p.Met1Lys
ENST00000494537.2:c.2T>A ENSP00000508308.1:p.Met1Lys