Canonical Allele Identifier: CA339111339

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25808579G>C , CM000663.2:g.25808579G>C	GRCh38
NC_000001.10:g.26135070G>C , CM000663.1:g.26135070G>C	GRCh37
NC_000001.9:g.26007657G>C	NCBI36
NG_009930.1:g.13404G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020451.3:c.538-1G>C MANE Select	NP_065184.2:n.538-1G>C
ENST00000361547.7:c.538-1G>C MANE Select	ENSP00000355141.2:n.538-1G>C
NM_020451.2:c.538-1G>C	NP_065184.2:n.538-1G>C
NM_206926.1:c.436-1G>C	NP_996809.1:n.436-1G>C
NM_206926.2:c.436-1G>C	NP_996809.1:n.436-1G>C
ENST00000354177.8:c.436-1G>C	ENSP00000346109.4:n.436-1G>C
ENST00000354177.9:c.436-1G>C	ENSP00000346109.5:n.436-1G>C
ENST00000361547.6:c.538-1G>C	ENSP00000355141.2:n.538-1G>C
ENST00000374315.1:c.436-1G>C	ENSP00000363434.1:n.436-1G>C
ENST00000494537.2:c.436-1G>C	ENSP00000508308.1:n.436-1G>C