Canonical Allele Identifier: CA710698169

Gene: SELENOS

Linked Data

• dbSNP Id: rs1462091190
• MyVariant Identifiers: chr15:g.101813918G>A (hg19) ; chr15:g.101273713G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101273713G>A , CM000677.2:g.101273713G>A	GRCh38
NC_000015.9:g.101813918G>A , CM000677.1:g.101813918G>A	GRCh37
NC_000015.8:g.99631441G>A	NCBI36
NG_013322.1:g.8783C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000526049.6:c.484+707C>T MANE Select	ENSP00000433541.1:n.484+707C>T
ENST00000398226.7:c.484+707C>T	ENSP00000381282.3:n.484+707C>T
ENST00000526043.1:n.1777+707C>T
ENST00000526049.5:c.484+707C>T	ENSP00000433541.1:n.484+707C>T
ENST00000528346.1:c.604+707C>T	ENSP00000434842.1:n.604+707C>T
ENST00000531964.5:c.415+707C>T	ENSP00000433803.1:n.415+707C>T
NM_018445.5:c.484+707C>T	NP_060915.2:n.484+707C>T
NM_203472.2:c.484+707C>T	NP_982298.2:n.484+707C>T
NM_018445.6:c.484+707C>T MANE Select	NP_060915.2:n.484+707C>T
NM_203472.3:c.484+707C>T	NP_982298.2:n.484+707C>T