Canonical Allele Identifier: CA10602788

Gene: SELENON

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25811533C>T , CM000663.2:g.25811533C>T	GRCh38
NC_000001.10:g.26138024C>T , CM000663.1:g.26138024C>T	GRCh37
NC_000001.9:g.26010611C>T	NCBI36
NG_009930.1:g.16358C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354177.9:c.919C>T	ENSP00000346109.5:p.Gln307Ter
ENST00000494537.2:c.988C>T	ENSP00000508308.1:p.Gln330Ter
ENST00000361547.7:c.1090C>T MANE Select	ENSP00000355141.2:p.Gln364Ter
ENST00000354177.8:c.988C>T	ENSP00000346109.4:p.Gln330Ter
ENST00000361547.6:c.1090C>T	ENSP00000355141.2:p.Gln364Ter
ENST00000374315.1:c.988C>T	ENSP00000363434.1:p.Gln330Ter
ENST00000559265.1:n.64C>T
NM_020451.2:c.1090C>T	NP_065184.2:p.Gln364Ter
NM_206926.1:c.988C>T	NP_996809.1:p.Gln330Ter
NM_020451.3:c.1090C>T MANE Select	NP_065184.2:p.Gln364Ter
NM_206926.2:c.988C>T	NP_996809.1:p.Gln330Ter