Canonical Allele Identifier: CA710698193

Gene: SELENOS

Linked Data

• dbSNP Id: rs979283317
• gnomAD v3: 15-101273731-C-G
• gnomAD v4: 15-101273731-C-G
• MyVariant Identifiers: chr15:g.101813936C>G (hg19) ; chr15:g.101273731C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101273731C>G , CM000677.2:g.101273731C>G	GRCh38
NC_000015.9:g.101813936C>G , CM000677.1:g.101813936C>G	GRCh37
NC_000015.8:g.99631459C>G	NCBI36
NG_013322.1:g.8765G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000526049.6:c.484+689G>C MANE Select	ENSP00000433541.1:n.484+689G>C
ENST00000398226.7:c.484+689G>C	ENSP00000381282.3:n.484+689G>C
ENST00000526043.1:n.1777+689G>C
ENST00000526049.5:c.484+689G>C	ENSP00000433541.1:n.484+689G>C
ENST00000528346.1:c.604+689G>C	ENSP00000434842.1:n.604+689G>C
ENST00000531964.5:c.415+689G>C	ENSP00000433803.1:n.415+689G>C
NM_018445.5:c.484+689G>C	NP_060915.2:n.484+689G>C
NM_203472.2:c.484+689G>C	NP_982298.2:n.484+689G>C
NM_018445.6:c.484+689G>C MANE Select	NP_060915.2:n.484+689G>C
NM_203472.3:c.484+689G>C	NP_982298.2:n.484+689G>C