Canonical Allele Identifier: CA620136134

Gene: SELENOS

Linked Data

• dbSNP Id: rs1268242961
• gnomAD v2: 15-101813349-T-A
• gnomAD v3: 15-101273144-T-A
• gnomAD v4: 15-101273144-T-A
• MyVariant Identifiers: chr15:g.101813349T>A (hg19) ; chr15:g.101273144T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101273144T>A , CM000677.2:g.101273144T>A	GRCh38
NC_000015.9:g.101813349T>A , CM000677.1:g.101813349T>A	GRCh37
NC_000015.8:g.99630872T>A	NCBI36
NG_013322.1:g.9352A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000526049.6:c.485-288A>T MANE Select	ENSP00000433541.1:n.485-288A>T
ENST00000398226.7:c.485-288A>T	ENSP00000381282.3:n.485-288A>T
ENST00000526043.1:n.1778-288A>T
ENST00000526049.5:c.485-288A>T	ENSP00000433541.1:n.485-288A>T
ENST00000528346.1:c.605-288A>T	ENSP00000434842.1:n.605-288A>T
ENST00000531964.5:c.416-288A>T	ENSP00000433803.1:n.416-288A>T
NM_018445.5:c.485-288A>T	NP_060915.2:n.485-288A>T
NM_203472.2:c.485-288A>T	NP_982298.2:n.485-288A>T
NM_018445.6:c.485-288A>T MANE Select	NP_060915.2:n.485-288A>T
NM_203472.3:c.485-288A>T	NP_982298.2:n.485-288A>T