Canonical Allele Identifier: CA2200446302

Gene: SELENOS

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101273671G= , CM000677.2:g.101273671G=	GRCh38
NC_000015.9:g.101813876G= , CM000677.1:g.101813876G=	GRCh37
NC_000015.8:g.99631399G=	NCBI36
NG_013322.1:g.8825C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000526049.6:c.484+749C= MANE Select	ENSP00000433541.1:n.484+749C=
ENST00000398226.7:c.484+749C=	ENSP00000381282.3:n.484+749C=
ENST00000526043.1:n.1777+749C=
ENST00000526049.5:c.484+749C=	ENSP00000433541.1:n.484+749C=
ENST00000528346.1:c.604+749C=	ENSP00000434842.1:n.604+749C=
ENST00000531964.5:c.415+749C=	ENSP00000433803.1:n.415+749C=
NM_018445.5:c.484+749C=	NP_060915.2:n.484+749C=
NM_203472.2:c.484+749C=	NP_982298.2:n.484+749C=
NM_018445.6:c.484+749C= MANE Select	NP_060915.2:n.484+749C=
NM_203472.3:c.484+749C=	NP_982298.2:n.484+749C=