Canonical Allele Identifier: CA276372382

Gene: SELENOS

Linked Data

• dbSNP Id: rs979425071
• gnomAD v2: 15-101813873-CA-C
• gnomAD v3: 15-101273668-CA-C
• gnomAD v4: 15-101273668-CA-C
• MyVariant Identifiers: chr15:g.101813874del (hg19) ; chr15:g.101273669del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101273670del , CM000677.2:g.101273670del	GRCh38
NC_000015.9:g.101813875del , CM000677.1:g.101813875del	GRCh37
NC_000015.8:g.99631398del	NCBI36
NG_013322.1:g.8827del

Transcript Alleles

HGVS	Amino-acid change
ENST00000526049.6:c.484+751del MANE Select	ENSP00000433541.1:n.484+751del
ENST00000398226.7:c.484+751del	ENSP00000381282.3:n.484+751del
ENST00000526043.1:n.1777+751del
ENST00000526049.5:c.484+751del	ENSP00000433541.1:n.484+751del
ENST00000528346.1:c.604+751del	ENSP00000434842.1:n.604+751del
ENST00000531964.5:c.415+751del	ENSP00000433803.1:n.415+751del
NM_018445.5:c.484+751del	NP_060915.2:n.484+751del
NM_203472.2:c.484+751del	NP_982298.2:n.484+751del
NM_018445.6:c.484+751del MANE Select	NP_060915.2:n.484+751del
NM_203472.3:c.484+751del	NP_982298.2:n.484+751del