Canonical Allele Identifier: CA2200446011

Gene: SELENOS

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101273049T= , CM000677.2:g.101273049T=	GRCh38
NC_000015.9:g.101813254T= , CM000677.1:g.101813254T=	GRCh37
NC_000015.8:g.99630777T=	NCBI36
NG_013322.1:g.9447A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000526049.6:c.485-193A= MANE Select	ENSP00000433541.1:n.485-193A=
ENST00000398226.7:c.485-193A=	ENSP00000381282.3:n.485-193A=
ENST00000526043.1:n.1778-193A=
ENST00000526049.5:c.485-193A=	ENSP00000433541.1:n.485-193A=
ENST00000528346.1:c.605-193A=	ENSP00000434842.1:n.605-193A=
ENST00000531964.5:c.416-193A=	ENSP00000433803.1:n.416-193A=
NM_018445.5:c.485-193A=	NP_060915.2:n.485-193A=
NM_203472.2:c.485-193A=	NP_982298.2:n.485-193A=
NM_018445.6:c.485-193A= MANE Select	NP_060915.2:n.485-193A=
NM_203472.3:c.485-193A=	NP_982298.2:n.485-193A=