Canonical Allele Identifier: CA2200446329

Gene: SELENOS

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101273721T= , CM000677.2:g.101273721T=	GRCh38
NC_000015.9:g.101813926T= , CM000677.1:g.101813926T=	GRCh37
NC_000015.8:g.99631449T=	NCBI36
NG_013322.1:g.8775A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000526049.6:c.484+699A= MANE Select	ENSP00000433541.1:n.484+699A=
ENST00000398226.7:c.484+699A=	ENSP00000381282.3:n.484+699A=
ENST00000526043.1:n.1777+699A=
ENST00000526049.5:c.484+699A=	ENSP00000433541.1:n.484+699A=
ENST00000528346.1:c.604+699A=	ENSP00000434842.1:n.604+699A=
ENST00000531964.5:c.415+699A=	ENSP00000433803.1:n.415+699A=
NM_018445.5:c.484+699A=	NP_060915.2:n.484+699A=
NM_203472.2:c.484+699A=	NP_982298.2:n.484+699A=
NM_018445.6:c.484+699A= MANE Select	NP_060915.2:n.484+699A=
NM_203472.3:c.484+699A=	NP_982298.2:n.484+699A=