Canonical Allele Identifier: CA696889

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25814000G>A , CM000663.2:g.25814000G>A	GRCh38
NC_000001.10:g.26140491G>A , CM000663.1:g.26140491G>A	GRCh37
NC_000001.9:g.26013078G>A	NCBI36
NG_009930.1:g.18825G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.1329+7G>A	ENSP00000346109.5:n.1329+7G>A
ENST00000494537.2:c.1487+7G>A	ENSP00000508308.1:n.1487+7G>A
ENST00000361547.7:c.1500+7G>A MANE Select	ENSP00000355141.2:n.1500+7G>A
ENST00000354177.8:c.1398+7G>A	ENSP00000346109.4:n.1398+7G>A
ENST00000361547.6:c.1500+7G>A	ENSP00000355141.2:n.1500+7G>A
ENST00000374315.1:c.1398+7G>A	ENSP00000363434.1:n.1398+7G>A
ENST00000494537.1:n.267+7G>A
ENST00000527604.1:c.21+7G>A	ENSP00000457066.1:n.21+7G>A
ENST00000559265.1:n.255+2121G>A
ENST00000630065.2:c.-73+7G>A	ENSP00000487549.1:n.-73+7G>A
NM_020451.2:c.1500+7G>A	NP_065184.2:n.1500+7G>A
NM_206926.1:c.1398+7G>A	NP_996809.1:n.1398+7G>A
NM_020451.3:c.1500+7G>A MANE Select	NP_065184.2:n.1500+7G>A
NM_206926.2:c.1398+7G>A	NP_996809.1:n.1398+7G>A