Canonical Allele Identifier: CA696841

Gene: SELENON

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25812780C>T , CM000663.2:g.25812780C>T	GRCh38
NC_000001.10:g.26139271C>T , CM000663.1:g.26139271C>T	GRCh37
NC_000001.9:g.26011858C>T	NCBI36
NG_009930.1:g.17605C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020451.3:c.1375C>T MANE Select	NP_065184.2:p.Gln459Ter
ENST00000361547.7:c.1375C>T MANE Select	ENSP00000355141.2:p.Gln459Ter
NM_020451.2:c.1375C>T	NP_065184.2:p.Gln459Ter
NM_206926.1:c.1273C>T	NP_996809.1:p.Gln425Ter
NM_206926.2:c.1273C>T	NP_996809.1:p.Gln425Ter
ENST00000354177.8:c.1273C>T	ENSP00000346109.4:p.Gln425Ter
ENST00000354177.9:c.1204C>T	ENSP00000346109.5:p.Gln402Ter
ENST00000361547.6:c.1375C>T	ENSP00000355141.2:p.Gln459Ter
ENST00000374315.1:c.1273C>T	ENSP00000363434.1:p.Gln425Ter
ENST00000494537.1:n.53C>T
ENST00000494537.2:c.1273C>T	ENSP00000508308.1:p.Gln425Ter
ENST00000559265.1:n.255+901C>T
ENST00000630065.2:c.-198C>T	ENSP00000487549.1:n.-198C>T