Canonical Allele Identifier: CA1159806116
Gene: SELENON HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25809004A= , CM000663.2:g.25809004A= GRCh38
NC_000001.10:g.26135495A= , CM000663.1:g.26135495A= GRCh37
NC_000001.9:g.26008082A= NCBI36
NG_009930.1:g.13829A=

Transcript Alleles

HGVS Amino-acid change
ENST00000354177.9:c.646-91A= ENSP00000346109.5:n.646-91A=
ENST00000494537.2:c.646-22A= ENSP00000508308.1:n.646-22A=
ENST00000361547.7:c.748-22A= MANE Select ENSP00000355141.2:n.748-22A=
ENST00000354177.8:c.646-22A= ENSP00000346109.4:n.646-22A=
ENST00000361547.6:c.748-22A= ENSP00000355141.2:n.748-22A=
ENST00000374315.1:c.646-22A= ENSP00000363434.1:n.646-22A=
NM_020451.2:c.748-22A= NP_065184.2:n.748-22A=
NM_206926.1:c.646-22A= NP_996809.1:n.646-22A=
NM_020451.3:c.748-22A= MANE Select NP_065184.2:n.748-22A=
NM_206926.2:c.646-22A= NP_996809.1:n.646-22A=