Canonical Allele Identifier: CA1145107027
Gene: SELENON HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809012C= , CM000663.2:g.25809012C= GRCh38
NC_000001.10:g.26135503C= , CM000663.1:g.26135503C= GRCh37
NC_000001.9:g.26008090C= NCBI36
NG_009930.1:g.13837C=

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.646-83C= ENSP00000346109.5:n.646-83C=
ENST00000494537.2:c.646-14C= ENSP00000508308.1:n.646-14C=
ENST00000361547.7:c.748-14C= MANE Select ENSP00000355141.2:n.748-14C=
ENST00000354177.8:c.646-14C= ENSP00000346109.4:n.646-14C=
ENST00000361547.6:c.748-14C= ENSP00000355141.2:n.748-14C=
ENST00000374315.1:c.646-14C= ENSP00000363434.1:n.646-14C=
NM_020451.2:c.748-14C= NP_065184.2:n.748-14C=
NM_206926.1:c.646-14C= NP_996809.1:n.646-14C=
NM_020451.3:c.748-14C= MANE Select NP_065184.2:n.748-14C=
NM_206926.2:c.646-14C= NP_996809.1:n.646-14C=