Canonical Allele Identifier: CA276371921

Gene: SELENOS

Linked Data

• dbSNP Id: rs539677677
• gnomAD v2: 15-101813343-A-T
• gnomAD v3: 15-101273138-A-T
• gnomAD v4: 15-101273138-A-T
• MyVariant Identifiers: chr15:g.101813343A>T (hg19) ; chr15:g.101273138A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101273138A>T , CM000677.2:g.101273138A>T	GRCh38
NC_000015.9:g.101813343A>T , CM000677.1:g.101813343A>T	GRCh37
NC_000015.8:g.99630866A>T	NCBI36
NG_013322.1:g.9358T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000526049.6:c.485-282T>A MANE Select	ENSP00000433541.1:n.485-282T>A
ENST00000398226.7:c.485-282T>A	ENSP00000381282.3:n.485-282T>A
ENST00000526043.1:n.1778-282T>A
ENST00000526049.5:c.485-282T>A	ENSP00000433541.1:n.485-282T>A
ENST00000528346.1:c.605-282T>A	ENSP00000434842.1:n.605-282T>A
ENST00000531964.5:c.416-282T>A	ENSP00000433803.1:n.416-282T>A
NM_018445.5:c.485-282T>A	NP_060915.2:n.485-282T>A
NM_203472.2:c.485-282T>A	NP_982298.2:n.485-282T>A
NM_018445.6:c.485-282T>A MANE Select	NP_060915.2:n.485-282T>A
NM_203472.3:c.485-282T>A	NP_982298.2:n.485-282T>A