Canonical Allele Identifier: CA276372351

Gene: SELENOS

Linked Data

• dbSNP Id: rs115491441
• gnomAD v2: 15-101813818-G-A
• gnomAD v3: 15-101273613-G-A
• gnomAD v4: 15-101273613-G-A
• MyVariant Identifiers: chr15:g.101813818G>A (hg19) ; chr15:g.101273613G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101273613G>A , CM000677.2:g.101273613G>A	GRCh38
NC_000015.9:g.101813818G>A , CM000677.1:g.101813818G>A	GRCh37
NC_000015.8:g.99631341G>A	NCBI36
NG_013322.1:g.8883C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000526049.6:c.485-757C>T MANE Select	ENSP00000433541.1:n.485-757C>T
ENST00000398226.7:c.485-757C>T	ENSP00000381282.3:n.485-757C>T
ENST00000526043.1:n.1778-757C>T
ENST00000526049.5:c.485-757C>T	ENSP00000433541.1:n.485-757C>T
ENST00000528346.1:c.605-757C>T	ENSP00000434842.1:n.605-757C>T
ENST00000531964.5:c.416-757C>T	ENSP00000433803.1:n.416-757C>T
NM_018445.5:c.485-757C>T	NP_060915.2:n.485-757C>T
NM_203472.2:c.485-757C>T	NP_982298.2:n.485-757C>T
NM_018445.6:c.485-757C>T MANE Select	NP_060915.2:n.485-757C>T
NM_203472.3:c.485-757C>T	NP_982298.2:n.485-757C>T