Canonical Allele Identifier: CA2644201138

Gene: SELENON

Linked Data

• gnomAD v4: 1-25812681-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812681C>A , CM000663.2:g.25812681C>A	GRCh38
NC_000001.10:g.26139172C>A , CM000663.1:g.26139172C>A	GRCh37
NC_000001.9:g.26011759C>A	NCBI36
NG_009930.1:g.17506C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000354177.9:c.1111-6C>A	ENSP00000346109.5:n.1111-6C>A
ENST00000494537.2:c.1180-6C>A	ENSP00000508308.1:n.1180-6C>A
ENST00000361547.7:c.1282-6C>A MANE Select	ENSP00000355141.2:n.1282-6C>A
ENST00000354177.8:c.1180-6C>A	ENSP00000346109.4:n.1180-6C>A
ENST00000361547.6:c.1282-6C>A	ENSP00000355141.2:n.1282-6C>A
ENST00000374315.1:c.1180-6C>A	ENSP00000363434.1:n.1180-6C>A
ENST00000559265.1:n.255+802C>A
NM_020451.2:c.1282-6C>A	NP_065184.2:n.1282-6C>A
NM_206926.1:c.1180-6C>A	NP_996809.1:n.1180-6C>A
NM_020451.3:c.1282-6C>A MANE Select	NP_065184.2:n.1282-6C>A
NM_206926.2:c.1180-6C>A	NP_996809.1:n.1180-6C>A