Canonical Allele Identifier: CA521739596

Gene: SELENON

Linked Data

• dbSNP Id: rs1422014692
• gnomAD v2: 1-26139172-C-T
• gnomAD v4: 1-25812681-C-T
• MyVariant Identifiers: chr1:g.26139172C>T (hg19) ; chr1:g.25812681C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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