Canonical Allele Identifier: CA999748154

Gene: SELENON

Linked Data

• gnomAD v3: 1-25812617-T-C
• gnomAD v4: 1-25812617-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812617T>C , CM000663.2:g.25812617T>C	GRCh38
NC_000001.10:g.26139108T>C , CM000663.1:g.26139108T>C	GRCh37
NC_000001.9:g.26011695T>C	NCBI36
NG_009930.1:g.17442T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1111-70T>C	ENSP00000346109.5:n.1111-70T>C
ENST00000494537.2:c.1180-70T>C	ENSP00000508308.1:n.1180-70T>C
ENST00000361547.7:c.1282-70T>C MANE Select	ENSP00000355141.2:n.1282-70T>C
ENST00000354177.8:c.1180-70T>C	ENSP00000346109.4:n.1180-70T>C
ENST00000361547.6:c.1282-70T>C	ENSP00000355141.2:n.1282-70T>C
ENST00000374315.1:c.1180-70T>C	ENSP00000363434.1:n.1180-70T>C
ENST00000559265.1:n.255+738T>C
NM_020451.2:c.1282-70T>C	NP_065184.2:n.1282-70T>C
NM_206926.1:c.1180-70T>C	NP_996809.1:n.1180-70T>C
NM_020451.3:c.1282-70T>C MANE Select	NP_065184.2:n.1282-70T>C
NM_206926.2:c.1180-70T>C	NP_996809.1:n.1180-70T>C